SIST EN 301 839-2 V1.3.1:2009
(Main)Electromagnetic compatibility and Radio spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz - Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive
- Abstract
The present document specifies requirements for ULP-AMI and peripherals including specific requirements for LBT and operating channel selection which external devices must use to select clear spectrum for a communications session. It is proposed to provide additional provisions to allow implanted devices to perform the LBT and operating channel selection functions for communications between implanted devices.
- Status
- Published
- Public Enquiry End Date
- 31-Mar-2009
- Publication Date
- 15-Nov-2009
- Technical Committee
- MOC - Mobile Communications
- Current Stage
- 6060 - National Implementation/Publication (Adopted Project)
- Start Date
- 20-Oct-2009
- Due Date
- 25-Dec-2009
- Completion Date
- 16-Nov-2009
- Mandate
- M/284
Buy Documents
ETSI EN 301 839-2 V1.3.1 (2009-01) - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive
ETSI EN 301 839-2 V1.3.1 (2009-07) - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive
ETSI EN 301 839-2 V1.3.1 (2009-10) - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive
SIST EN 301 839-2 V1.3.1:2009 is the SIST adoption of the ETSI harmonized European standard for short range devices used as Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) in the 402 MHz to 405 MHz band. It specifies the radio spectrum and electromagnetic compatibility requirements used to show conformity with Article 3.2 of the R&TTE Directive, mainly for manufacturers, test labs, and conformity assessors working on implanted medical radio equipment.
What does SIST EN 301 839-2 V1.3.1:2009 specify?
SIST EN 301 839-2 V1.3.1:2009 specifies the essential radio requirements for ULP-AMI and ULP-AMI-P equipment operating in all or part of the 402 MHz to 405 MHz range. The standard is focused on spectrum use, interference control, and the test evidence needed for conformity.
The document is organized into five clauses and three annexes.
| Annex | What it covers |
|---|---|
| Annex A | HS Requirements and conformance Test specifications Table (HS-RTT) for presumption of conformity |
| Annex B | EN title in the official languages |
| Annex C | Bibliography |
Clause 1 states the scope, Clause 2 lists references, Clause 3 gives definitions and abbreviations, Clause 4 sets the technical requirements and specifications, and Clause 5 gives the compliance testing approach.
What are the key requirements of SIST EN 301 839-2 V1.3.1:2009?
SIST EN 301 839-2 V1.3.1:2009 ties compliance to both equipment design and radio performance. In practice, a manufacturer must declare how the device operates, then verify that the device stays within the declared operating conditions and limits.
- Environmental profile, Clause 4.1 - The manufacturer declares the operational environmental profile, and the equipment must meet the requirements within that declared range. This matters because testing has to reflect the real temperature, humidity, and other conditions under which the implant or peripheral will be used.
- Mechanical and electrical design, Clause 4.2.1 - The equipment must be designed with sound engineering practice to minimize harmful interference. Antennas are restricted to integral or dedicated types, user-accessible controls that could worsen interference should be protected, and any automatic transmitter shut-off or battery-saving feature may need to be disabled for testing.
- Radio performance, Clauses 4.2.2 to 4.2.7 - The standard requires compliance for frequency error, emission bandwidth, effective radiated power of the fundamental emission, transmitter spurious emissions, frequency stability under low voltage conditions, and receiver spurious radiation. The limits and definitions are taken from EN 301 839-1, so part 2 mainly tells you which items must be checked for Article 3.2 conformity.
- Spectrum access, Clause 4.2.8 - The manufacturer must declare a spectrum access method. At least one method must be chosen: LBT/AFA or LP/LDC. Both methods may be implemented, but operating with both is only allowed when the total emission bandwidth does not exceed 300 kHz. This is important because the access method affects how the device finds and uses a clear channel.
- LP/LDC applicability, Clause 4.2.8.2 - The LP/LDC requirement applies only to ULP-AMI accessing the 403.5 MHz to 403.8 MHz band. For buyers and engineers, this means the chosen operating mode must match the intended band and device type.
- Testing and uncertainty, Clause 5 - Tests are performed at representative points within the declared environmental profile, and the test report must include measurement uncertainty. The uncertainty values are based on TR 100 028. This matters because compliance is judged from measured values against the limits, not from nominal design claims.
- Essential Radio Test Suite, Annex A and Clause 5.3 - The HS-RTT identifies which requirements are unconditional or conditional and which tests are Essential. For presumption of conformity, the Essential tests are the ones that must be demonstrated with the referenced procedures.
What terms does SIST EN 301 839-2 V1.3.1:2009 define?
The standard uses the definitions and abbreviations from EN 301 839-1, so part 1 is the glossary for this part.
- Ultra Low Power Active Medical Implant (ULP-AMI) - An implanted medical radio device operating in the 402 MHz to 405 MHz range.
- Ultra Low Power Active Medical Implant Peripheral (ULP-AMI-P) - A peripheral device associated with ULP-AMI equipment in the same frequency range.
- Listen Before Talk (LBT) - A spectrum access method where the device checks the channel before transmitting.
- Adaptive Frequency Agility (AFA) - The companion access method used with LBT in the monitoring-system approach.
- Low Power/Low Duty Cycle (LP/LDC) - A spectrum access method based on restricted power and duty cycle.
- Monitoring system - The circuitry in a medical implant transmitter or ULP-AMI-P that supports the LBT and AFA spectrum access protocol.
- Effective radiated power - The transmitted power measure used in the conformity checks for the fundamental emission.
Who uses SIST EN 301 839-2 V1.3.1:2009?
SIST EN 301 839-2 V1.3.1:2009 is used by manufacturers of implanted medical radio devices and their peripherals, especially when selecting antennas, channel access methods, and shutdown features. It is also used by RF design engineers, test laboratories, and compliance teams that need to run the essential radio tests and document measurement uncertainty.
Quality managers, conformity assessors, and certification teams use the HS-RTT in Annex A to map each requirement to its test status. Regulatory and procurement teams use it to check whether a device has the technical evidence needed for Article 3.2 conformity.
Which standards are used with SIST EN 301 839-2 V1.3.1:2009?
The main companion standard is ETSI EN 301 839-1 (V1.3.1). It provides the technical characteristics, definitions, limits, and detailed test methods that part 2 refers to for frequency error, bandwidth, power, emissions, low-voltage stability, and spectrum access.
The standard also uses ETSI TR 100 028 (V1.4.1) for the treatment of measurement uncertainty. That reference matters because Clause 5.2 requires uncertainty values in the test report and links their calculation to that technical report.
What does the SIST EN 301 839-2 V1.3.1:2009 document contain?
The document contains the scope, references, definitions, technical requirements, and compliance testing rules for ULP-AMI and ULP-AMI-P equipment. Clause 4 is the main requirements section, while Clause 5 explains how to test the equipment and how to interpret results.
It also includes Table 1 with the transmit and receive service bands, Table 2 with maximum measurement uncertainty values, and Annex A with the HS-RTT used for presumption of conformity. Annex B gives the EN title in official languages, and Annex C lists background references.
Buy Documents
ETSI EN 301 839-2 V1.3.1 (2009-01) - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive
ETSI EN 301 839-2 V1.3.1 (2009-07) - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive
ETSI EN 301 839-2 V1.3.1 (2009-10) - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive
Get Certified
Connect with accredited certification bodies for this standard
BSI Group
BSI (British Standards Institution) is the business standards company that helps organizations make excellence a habit.
TÜV Rheinland
TÜV Rheinland is a leading international provider of technical services.
TÜV SÜD
TÜV SÜD is a trusted partner of choice for safety, security and sustainability solutions.
Sponsored listings
Frequently Asked Questions
SIST EN 301 839-2 V1.3.1:2009 is a standard published by the Slovenian Institute for Standardization (SIST). Its full title is "Electromagnetic compatibility and Radio spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz - Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive". This standard covers: The present document specifies requirements for ULP-AMI and peripherals including specific requirements for LBT and operating channel selection which external devices must use to select clear spectrum for a communications session. It is proposed to provide additional provisions to allow implanted devices to perform the LBT and operating channel selection functions for communications between implanted devices.
The present document specifies requirements for ULP-AMI and peripherals including specific requirements for LBT and operating channel selection which external devices must use to select clear spectrum for a communications session. It is proposed to provide additional provisions to allow implanted devices to perform the LBT and operating channel selection functions for communications between implanted devices.
SIST EN 301 839-2 V1.3.1:2009 is classified under the following ICS (International Classification for Standards) categories: 11.040.40 - Implants for surgery, prosthetics and orthotics; 33.060.20 - Receiving and transmitting equipment; 33.100.01 - Electromagnetic compatibility in general. The ICS classification helps identify the subject area and facilitates finding related standards.
SIST EN 301 839-2 V1.3.1:2009 is associated with the following European legislation: EU Directives/Regulations: 1999/5/EC, TRRTP124; Standardization Mandates: M/284. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
SIST EN 301 839-2 V1.3.1:2009 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
Draft ETSI EN 301 839-2 V1.3.1 (2009-01)
Harmonized European Standard (Telecommunications series)
Electromagnetic compatibility
and Radio spectrum Matters (ERM);
Short Range Devices (SRD);
Ultra Low Power Active Medical Implants (ULP-AMI)
and Peripherals (ULP-AMI-P)
operating in the frequency range 402 MHz to 405 MHz;
Part 2: Harmonized EN covering essential requirements
of article 3.2 of the R&TTE Directive
2 Draft ETSI EN 301 839-2 V1.3.1 (2009-01)
Reference
REN/ERM-TG30-263-2
Keywords
radio, regulation, SRD, testing
ETSI
650 Route des Lucioles
F-06921 Sophia Antipolis Cedex - FRANCE
Tel.: +33 4 92 94 42 00 Fax: +33 4 93 65 47 16
Siret N° 348 623 562 00017 - NAF 742 C
Association à but non lucratif enregistrée à la
Sous-Préfecture de Grasse (06) N° 7803/88
Important notice
Individual copies of the present document can be downloaded from:
http://www.etsi.org
The present document may be made available in more than one electronic version or in print. In any case of existing or
perceived difference in contents between such versions, the reference version is the Portable Document Format (PDF).
In case of dispute, the reference shall be the printing on ETSI printers of the PDF version kept on a specific network drive
within ETSI Secretariat.
Users of the present document should be aware that the document may be subject to revision or change of status.
Information on the current status of this and other ETSI documents is available at
http://portal.etsi.org/tb/status/status.asp
If you find errors in the present document, please send your comment to one of the following services:
http://portal.etsi.org/chaircor/ETSI_support.asp
Copyright Notification
No part may be reproduced except as authorized by written permission.
The copyright and the foregoing restriction extend to reproduction in all media.
© European Telecommunications Standards Institute 2009.
All rights reserved.
TM TM TM TM
DECT , PLUGTESTS , UMTS , TIPHON , the TIPHON logo and the ETSI logo are Trade Marks of ETSI registered
for the benefit of its Members.
TM
3GPP is a Trade Mark of ETSI registered for the benefit of its Members and of the 3GPP Organizational Partners.
LTE™ is a Trade Mark of ETSI currently being registered
for the benefit of its Members and of the 3GPP Organizational Partners.
GSM® and the GSM logo are Trade Marks registered and owned by the GSM Association.
ETSI
3 Draft ETSI EN 301 839-2 V1.3.1 (2009-01)
Contents
Intellectual Property Rights . 5
Foreword . 5
1 Scope . 6
2 References . 6
2.1 Normative references . 7
2.2 Informative references . 7
3 Definitions and abbreviations . 7
3.1 Definitions . 7
3.2 Abbreviations . 7
4 Technical requirements and specifications . 7
4.1 Environmental profile . 7
4.2 Conformance requirements . 8
4.2.1 Mechanical and electrical design . 8
4.2.1.1 General . 8
4.2.1.2 Antennas . 8
4.2.1.3 Controls . 8
4.2.1.4 Transmitter shut-off facility . 8
4.2.2 Frequency error . 8
4.2.2.1 Definition . 8
4.2.2.2 Limits . 8
4.2.2.3 Conformance . 8
4.2.3 Emission bandwidth . 8
4.2.3.1 Definition . 8
4.2.3.2 Limits . 8
4.2.3.3 Conformance . 8
4.2.4 Effective radiated power of the fundamental emission . 9
4.2.4.1 Definition . 9
4.2.4.2 Limits . 9
4.2.4.3 Conformance . 9
4.2.5 Spurious emissions of transmitter . 9
4.2.5.1 Definition . 9
4.2.5.2 Limits . 9
4.2.5.3 Conformance . 9
4.2.6 Frequency stability under low voltage conditions . 9
4.2.6.1 Definition . 9
4.2.6.2 Limits . 9
4.2.6.3 Conformance . 9
4.2.7 Spurious radiation of receivers . 9
4.2.7.1 Definition . 9
4.2.7.2 Limits . 9
4.2.7.3 Conformance . 9
4.2.8 Spectrum Access . 10
4.2.8.1 LBT/AFA spectrum access . 10
4.2.8.1.1 Definition. 10
4.2.8.1.2 Limits . 10
4.2.8.2 LP/LDC spectrum access . 10
4.2.8.2.1 Definition. 10
4.2.8.2.2 Limits . 10
4.2.8.3 Conformance . 10
5 Testing for compliance with technical requirements . 11
5.1 Environmental conditions for testing . 11
5.2 Interpretation of the measurement results . 11
5.3 Essential radio test suites . 11
ETSI
4 Draft ETSI EN 301 839-2 V1.3.1 (2009-01)
5.3.1 Frequency error . 11
5.3.2 Emission bandwidth . 12
5.3.3 Effective radiated power of the fundamental emission . 12
5.3.4 Spurious emissions of transmitter . 12
5.3.5 Frequency stability under low voltage conditions . 12
5.3.6 Spurious radiation of receivers . 12
5.3.7 Spectrum Access . 12
5.3.7.1 LBT/AFA spectrum access . 12
5.3.7.2 LP/LDC spectrum access . 12
5.3.8 Normal and extreme test-conditions . 12
5.3.9 Test power source . 12
5.3.10 Choice of samples for test suites . 12
Annex A (normative): HS Requirements and conformance Test specifications Table
(HS-RTT) . 13
Annex B (informative): The EN title in the official languages . 15
Annex C (informative): Bibliography . 16
History . 17
ETSI
5 Draft ETSI EN 301 839-2 V1.3.1 (2009-01)
Intellectual Property Rights
IPRs essential or potentially essential to the present document may have been declared to ETSI. The information
pertaining to these essential IPRs, if any, is publicly available for ETSI members and non-members, and can be found
in ETSI SR 000 314: "Intellectual Property Rights (IPRs); Essential, or potentially Essential, IPRs notified to ETSI in
respect of ETSI standards", which is available from the ETSI Secretariat. Latest updates are available on the ETSI Web
server (http://webapp.etsi.org/IPR/home.asp).
Pursuant to the ETSI IPR Policy, no investigation, including IPR searches, has been carried out by ETSI. No guarantee
can be given as to the existence of other IPRs not referenced in ETSI SR 000 314 (or the updates on the ETSI Web
server) which are, or may be, or may become, essential to the present document.
Foreword
This Harmonized European Standard (Telecommunications series) has been produced by ETSI Technical Committee
Electromagnetic compatibility and Radio spectrum Matters (ERM), and is now submitted for the Public Enquiry phase
of the ETSI standards Two-step Approval Procedure.
The present document has been produced by ETSI in response to a mandate from the European Commission issued
under Council Directive 98/34/EC (as amended) [i.3] laying down a procedure for the provision of information in the
field of technical standards and regulations.
The present document is intended to become a Harmonized Standard, the reference of which will be published in the
Official Journal of the European Communities referencing the Directive 1999/5/EC [i.1] of the European Parliament
and of the Council of 9 March 1999 on radio equipment and telecommunications terminal equipment and the mutual
recognition of their conformity ("the R&TTE Directive") [i.1].
Technical specifications relevant to Directive 1999/5/EC [i.1] are given in annex A.
The present document is part 2 of a multi-part deliverable covering Short Range Devices (SRD); Ultra Low Power
Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to
405 MHz, as identified below:
Part 1: "Technical characteristics and test methods";
Part 2: "Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive".
Proposed national transposition dates
Date of latest announcement of this EN (doa): 3 months after ETSI publication
Date of latest publication of new National Standard
or endorsement of this EN (dop/e): 6 months after doa
Date of withdrawal of any conflicting National Standard (dow): 18 months after doa
ETSI
6 Draft ETSI EN 301 839-2 V1.3.1 (2009-01)
1 Scope
The present document applies to the following radio equipment types:
• Ultra Low Power Active Medical Implants (ULP-AMI);
• and Peripherals (ULP-AMI-P).
These radio equipment types are capable of operating in all or any part of the frequency bands in table 1.
Table 1: Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Transmit Ultra Low Power Active Medical Implants 402 MHz to 405 MHz
(ULP-AMI) and Peripherals (ULP-AMI-P)
Receive Ultra Low Power Active Medical Implants 402 MHz to 405 MHz
(ULP-AMI) and Peripherals (ULP-AMI-P)
The present document is intended to cover the provisions of Directive 1999/5/EC [i.1] (R&TTE Directive).
Article 3.2, which states that "…. radio equipment shall be so constructed that it effectively uses the spectrum allocated
to terrestrial/space radio communications and orbital resources so as to avoid harmful interference".
An AIMD is regulated under the AIMD Directive 90/385/EEC [i.2]: radio parts contained therein (referred to herein as
ULP-AMI and ULP-AMI-P for peripheral devices) are regulated under the Directive 1999/5/EC [i.1].
In addition to the present document, other ENs that specify technical requirements in respect of essential requirements
under other parts of Article 3 of the R&TTE Directive [i.1] may apply to equipment within the scope of the present
document.
NOTE: A list of such ENs is included on the web site http://www.newapproach.org.
2 References
References are either specific (identified by date of publication and/or edition number or version number) or
non-specific.
• For a specific reference, subsequent revisions do not apply.
• Non-specific reference may be made only to a complete document or a part thereof and only in the following
cases:
- if it is accepted that it will be possible to use all future changes of the referenced document for the
purposes of the referring document;
- for informative references.
Referenced documents which are not found to be publicly available in the expected location might be found at
http://docbox.etsi.org/Reference.
For online referenced documents, information sufficient to identify and locate the source shall be provided. Preferably,
the primary source of the referenced document should be cited, in order to ensure traceability. Furthermore, the
reference should, as far as possible, remain valid for the expected life of the document. The reference shall include the
method of access to the referenced document and the full network address, with the same punctuation and use of upper
case and lower case letters.
NOTE: While any hyperlinks included in this clause were valid at the time of publication ETSI cannot guarantee
their long term validity.
ETSI
...
Final draft ETSI EN 301 839-2 V1.3.1 (2009-07)
Harmonized European Standard (Telecommunications series)
Electromagnetic compatibility
and Radio spectrum Matters (ERM);
Short Range Devices (SRD);
Ultra Low Power Active Medical Implants (ULP-AMI)
and Peripherals (ULP-AMI-P)
operating in the frequency range 402 MHz to 405 MHz;
Part 2: Harmonized EN covering essential requirements
of article 3.2 of the R&TTE Directive
2 Final draft ETSI EN 301 839-2 V1.3.1 (2009-07)
Reference
REN/ERM-TG30-263-2
Keywords
radio, regulation, SRD, testing
ETSI
650 Route des Lucioles
F-06921 Sophia Antipolis Cedex - FRANCE
Tel.: +33 4 92 94 42 00 Fax: +33 4 93 65 47 16
Siret N° 348 623 562 00017 - NAF 742 C
Association à but non lucratif enregistrée à la
Sous-Préfecture de Grasse (06) N° 7803/88
Important notice
Individual copies of the present document can be downloaded from:
http://www.etsi.org
The present document may be made available in more than one electronic version or in print. In any case of existing or
perceived difference in contents between such versions, the reference version is the Portable Document Format (PDF).
In case of dispute, the reference shall be the printing on ETSI printers of the PDF version kept on a specific network drive
within ETSI Secretariat.
Users of the present document should be aware that the document may be subject to revision or change of status.
Information on the current status of this and other ETSI documents is available at
http://portal.etsi.org/tb/status/status.asp
If you find errors in the present document, please send your comment to one of the following services:
http://portal.etsi.org/chaircor/ETSI_support.asp
Copyright Notification
No part may be reproduced except as authorized by written permission.
The copyright and the foregoing restriction extend to reproduction in all media.
© European Telecommunications Standards Institute 2009.
All rights reserved.
TM TM TM TM
DECT , PLUGTESTS , UMTS , TIPHON , the TIPHON logo and the ETSI logo are Trade Marks of ETSI registered
for the benefit of its Members.
TM
3GPP is a Trade Mark of ETSI registered for the benefit of its Members and of the 3GPP Organizational Partners.
LTE™ is a Trade Mark of ETSI currently being registered
for the benefit of its Members and of the 3GPP Organizational Partners.
GSM® and the GSM logo are Trade Marks registered and owned by the GSM Association.
ETSI
3 Final draft ETSI EN 301 839-2 V1.3.1 (2009-07)
Contents
Intellectual Property Rights . 5
Foreword . 5
1 Scope . 6
2 References . 6
2.1 Normative references . 7
2.2 Informative references . 7
3 Definitions and abbreviations . 7
3.1 Definitions . 7
3.2 Abbreviations . 7
4 Technical requirements and specifications . 7
4.1 Environmental profile . 7
4.2 Conformance requirements . 8
4.2.1 Mechanical and electrical design . 8
4.2.1.1 General . 8
4.2.1.2 Antennas . 8
4.2.1.3 Controls . 8
4.2.1.4 Transmitter shut-off facility . 8
4.2.2 Frequency error . 8
4.2.2.1 Definition . 8
4.2.2.2 Limits . 8
4.2.2.3 Conformance . 8
4.2.3 Emission bandwidth . 8
4.2.3.1 Definition . 8
4.2.3.2 Limits . 8
4.2.3.3 Conformance . 8
4.2.4 Effective radiated power of the fundamental emission . 9
4.2.4.1 Definition . 9
4.2.4.2 Limits . 9
4.2.4.3 Conformance . 9
4.2.5 Spurious emissions of transmitter . 9
4.2.5.1 Definition . 9
4.2.5.2 Limits . 9
4.2.5.3 Conformance . 9
4.2.6 Frequency stability under low voltage conditions . 9
4.2.6.1 Definition . 9
4.2.6.2 Limits . 9
4.2.6.3 Conformance . 9
4.2.7 Spurious radiation of receivers . 9
4.2.7.1 Definition . 9
4.2.7.2 Limits . 9
4.2.7.3 Conformance . 9
4.2.8 Spectrum Access . 10
4.2.8.1 LBT/AFA spectrum access . 10
4.2.8.1.1 Definition. 10
4.2.8.1.2 Limits . 10
4.2.8.2 LP/LDC spectrum access . 10
4.2.8.2.1 Definition. 10
4.2.8.2.2 Limits . 10
4.2.8.3 Conformance . 10
5 Testing for compliance with technical requirements . 11
5.1 Environmental conditions for testing . 11
5.2 Interpretation of the measurement results . 11
5.3 Essential radio test suites . 11
ETSI
4 Final draft ETSI EN 301 839-2 V1.3.1 (2009-07)
5.3.1 Frequency error . 11
5.3.2 Emission bandwidth . 12
5.3.3 Effective radiated power of the fundamental emission . 12
5.3.4 Spurious emissions of transmitter . 12
5.3.5 Frequency stability under low voltage conditions . 12
5.3.6 Spurious radiation of receivers . 12
5.3.7 Spectrum Access . 12
5.3.7.1 LBT/AFA spectrum access . 12
5.3.7.2 LP/LDC spectrum access . 12
5.3.8 Normal and extreme test-conditions . 12
5.3.9 Test power source . 12
5.3.10 Choice of samples for test suites . 12
Annex A (normative): HS Requirements and conformance Test specifications Table
(HS-RTT) . 13
Annex B (informative): The EN title in the official languages . 15
Annex C (informative): Bibliography . 16
History . 17
ETSI
5 Final draft ETSI EN 301 839-2 V1.3.1 (2009-07)
Intellectual Property Rights
IPRs essential or potentially essential to the present document may have been declared to ETSI. The information
pertaining to these essential IPRs, if any, is publicly available for ETSI members and non-members, and can be found
in ETSI SR 000 314: "Intellectual Property Rights (IPRs); Essential, or potentially Essential, IPRs notified to ETSI in
respect of ETSI standards", which is available from the ETSI Secretariat. Latest updates are available on the ETSI Web
server (http://webapp.etsi.org/IPR/home.asp).
Pursuant to the ETSI IPR Policy, no investigation, including IPR searches, has been carried out by ETSI. No guarantee
can be given as to the existence of other IPRs not referenced in ETSI SR 000 314 (or the updates on the ETSI Web
server) which are, or may be, or may become, essential to the present document.
Foreword
This Harmonized European Standard (Telecommunications series) has been produced by ETSI Technical Committee
Electromagnetic compatibility and Radio spectrum Matters (ERM), and is now submitted for the Vote phase of the
ETSI standards Two-step Approval Procedure.
The present document has been produced by ETSI in response to a mandate from the European Commission issued
under Council Directive 98/34/EC (as amended) [i.3] laying down a procedure for the provision of information in the
field of technical standards and regulations.
The present document is intended to become a Harmonized Standard, the reference of which will be published in the
Official Journal of the European Communities referencing the Directive 1999/5/EC [i.1] of the European Parliament
and of the Council of 9 March 1999 on radio equipment and telecommunications terminal equipment and the mutual
recognition of their conformity ("the R&TTE Directive") [i.1].
Technical specifications relevant to Directive 1999/5/EC [i.1] are given in annex A.
The present document is part 2 of a multi-part deliverable covering Short Range Devices (SRD); Ultra Low Power
Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to
405 MHz, as identified below:
Part 1: "Technical characteristics and test methods";
Part 2: "Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive".
Proposed national transposition dates
Date of latest announcement of this EN (doa): 3 months after ETSI publication
Date of latest publication of new National Standard
or endorsement of this EN (dop/e): 6 months after doa
Date of withdrawal of any conflicting National Standard (dow): 18 months after doa
ETSI
6 Final draft ETSI EN 301 839-2 V1.3.1 (2009-07)
1 Scope
The present document applies to the following radio equipment types:
• Ultra Low Power Active Medical Implants (ULP-AMI);
• and Peripherals (ULP-AMI-P).
These radio equipment types are capable of operating in all or any part of the frequency bands in table 1.
Table 1: Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Transmit Ultra Low Power Active Medical Implants 402 MHz to 405 MHz
(ULP-AMI) and Peripherals (ULP-AMI-P)
Receive Ultra Low Power Active Medical Implants 402 MHz to 405 MHz
(ULP-AMI) and Peripherals (ULP-AMI-P)
The present document is intended to cover the provisions of Directive 1999/5/EC [i.1] (R&TTE Directive), Article 3.2,
which states that "…. radio equipment shall be so constructed that it effectively uses the spectrum allocated to
terrestrial/space radio communications and orbital resources so as to avoid harmful interference".
An AIMD is regulated under the AIMD Directive 90/385/EEC [i.2]: radio parts contained therein (referred to herein as
ULP-AMI and ULP-AMI-P for peripheral devices) are regulated under the Directive 1999/5/EC [i.1].
In addition to the present document, other ENs that specify technical requirements in respect of essential requirements
under other parts of Article 3 of the R&TTE Directive [i.1] may apply to equipment within the scope of the present
document.
NOTE: A list of such ENs is included on the web site http://www.newapproach.org.
2 References
References are either specific (identified by date of publication and/or edition number or version number) or
non-specific.
• For a specific reference, subsequent revisions do not apply.
• Non-specific reference may be made only to a complete document or a part thereof and only in the following
cases:
- if it is accepted that it will be possible to use all future changes of the referenced document for the
purposes of the referring document;
- for informative references.
Referenced documents which are not found to be publicly available in the expected location might be found at
http://docbox.etsi.org/Reference.
NOTE: While any hyperlinks included in this clause were valid at the time of publication ETSI cannot guarantee
their long term validity.
ETSI
7 Final draft ETSI EN 301 839-2 V1.3.1 (2009-07)
2.1 Normative references
The following referenced documents are indispensable for the application of the present document. For dated
references, only the edition cited applies. For non-specific references, the latest ed
...
Harmonized European Standard (Telecommunications series)
Electromagnetic compatibility
and Radio spectrum Matters (ERM);
Short Range Devices (SRD);
Ultra Low Power Active Medical Implants (ULP-AMI)
and Peripherals (ULP-AMI-P)
operating in the frequency range 402 MHz to 405 MHz;
Part 2: Harmonized EN covering essential requirements
of article 3.2 of the R&TTE Directive
2 ETSI EN 301 839-2 V1.3.1 (2009-10)
Reference
REN/ERM-TG30-263-2
Keywords
radio, regulation, SRD, testing
ETSI
650 Route des Lucioles
F-06921 Sophia Antipolis Cedex - FRANCE
Tel.: +33 4 92 94 42 00 Fax: +33 4 93 65 47 16
Siret N° 348 623 562 00017 - NAF 742 C
Association à but non lucratif enregistrée à la
Sous-Préfecture de Grasse (06) N° 7803/88
Important notice
Individual copies of the present document can be downloaded from:
http://www.etsi.org
The present document may be made available in more than one electronic version or in print. In any case of existing or
perceived difference in contents between such versions, the reference version is the Portable Document Format (PDF).
In case of dispute, the reference shall be the printing on ETSI printers of the PDF version kept on a specific network drive
within ETSI Secretariat.
Users of the present document should be aware that the document may be subject to revision or change of status.
Information on the current status of this and other ETSI documents is available at
http://portal.etsi.org/tb/status/status.asp
If you find errors in the present document, please send your comment to one of the following services:
http://portal.etsi.org/chaircor/ETSI_support.asp
Copyright Notification
No part may be reproduced except as authorized by written permission.
The copyright and the foregoing restriction extend to reproduction in all media.
© European Telecommunications Standards Institute 2009.
All rights reserved.
TM TM TM TM
DECT , PLUGTESTS , UMTS , TIPHON , the TIPHON logo and the ETSI logo are Trade Marks of ETSI registered
for the benefit of its Members.
TM
3GPP is a Trade Mark of ETSI registered for the benefit of its Members and of the 3GPP Organizational Partners.
LTE™ is a Trade Mark of ETSI currently being registered
for the benefit of its Members and of the 3GPP Organizational Partners.
GSM® and the GSM logo are Trade Marks registered and owned by the GSM Association.
ETSI
3 ETSI EN 301 839-2 V1.3.1 (2009-10)
Contents
Intellectual Property Rights . 5
Foreword . 5
1 Scope . 6
2 References . 6
2.1 Normative references . 7
2.2 Informative references . 7
3 Definitions and abbreviations . 7
3.1 Definitions . 7
3.2 Abbreviations . 7
4 Technical requirements and specifications . 7
4.1 Environmental profile . 7
4.2 Conformance requirements . 8
4.2.1 Mechanical and electrical design . 8
4.2.1.1 General . 8
4.2.1.2 Antennas . 8
4.2.1.3 Controls . 8
4.2.1.4 Transmitter shut-off facility . 8
4.2.2 Frequency error . 8
4.2.2.1 Definition . 8
4.2.2.2 Limits . 8
4.2.2.3 Conformance . 8
4.2.3 Emission bandwidth . 8
4.2.3.1 Definition . 8
4.2.3.2 Limits . 8
4.2.3.3 Conformance . 8
4.2.4 Effective radiated power of the fundamental emission . 9
4.2.4.1 Definition . 9
4.2.4.2 Limits . 9
4.2.4.3 Conformance . 9
4.2.5 Spurious emissions of transmitter . 9
4.2.5.1 Definition . 9
4.2.5.2 Limits . 9
4.2.5.3 Conformance . 9
4.2.6 Frequency stability under low voltage conditions . 9
4.2.6.1 Definition . 9
4.2.6.2 Limits . 9
4.2.6.3 Conformance . 9
4.2.7 Spurious radiation of receivers . 9
4.2.7.1 Definition . 9
4.2.7.2 Limits . 9
4.2.7.3 Conformance . 9
4.2.8 Spectrum Access . 10
4.2.8.1 LBT/AFA spectrum access . 10
4.2.8.1.1 Definition. 10
4.2.8.1.2 Limits . 10
4.2.8.2 LP/LDC spectrum access . 10
4.2.8.2.1 Definition. 10
4.2.8.2.2 Limits . 10
4.2.8.3 Conformance . 10
5 Testing for compliance with technical requirements . 11
5.1 Environmental conditions for testing . 11
5.2 Interpretation of the measurement results . 11
5.3 Essential radio test suites . 11
ETSI
4 ETSI EN 301 839-2 V1.3.1 (2009-10)
5.3.1 Frequency error . 11
5.3.2 Emission bandwidth . 12
5.3.3 Effective radiated power of the fundamental emission . 12
5.3.4 Spurious emissions of transmitter . 12
5.3.5 Frequency stability under low voltage conditions . 12
5.3.6 Spurious radiation of receivers . 12
5.3.7 Spectrum Access . 12
5.3.7.1 LBT/AFA spectrum access . 12
5.3.7.2 LP/LDC spectrum access . 12
5.3.8 Normal and extreme test-conditions . 12
5.3.9 Test power source . 12
5.3.10 Choice of samples for test suites . 12
Annex A (normative): HS Requirements and conformance Test specifications Table
(HS-RTT) . 13
Annex B (informative): The EN title in the official languages . 15
Annex C (informative): Bibliography . 16
History . 17
ETSI
5 ETSI EN 301 839-2 V1.3.1 (2009-10)
Intellectual Property Rights
IPRs essential or potentially essential to the present document may have been declared to ETSI. The information
pertaining to these essential IPRs, if any, is publicly available for ETSI members and non-members, and can be found
in ETSI SR 000 314: "Intellectual Property Rights (IPRs); Essential, or potentially Essential, IPRs notified to ETSI in
respect of ETSI standards", which is available from the ETSI Secretariat. Latest updates are available on the ETSI Web
server (http://webapp.etsi.org/IPR/home.asp).
Pursuant to the ETSI IPR Policy, no investigation, including IPR searches, has been carried out by ETSI. No guarantee
can be given as to the existence of other IPRs not referenced in ETSI SR 000 314 (or the updates on the ETSI Web
server) which are, or may be, or may become, essential to the present document.
Foreword
This Harmonized European Standard (Telecommunications series) has been produced by ETSI Technical Committee
Electromagnetic compatibility and Radio spectrum Matters (ERM).
The present document has been produced by ETSI in response to a mandate from the European Commission issued
under Council Directive 98/34/EC (as amended) [i.3] laying down a procedure for the provision of information in the
field of technical standards and regulations.
The present document is intended to become a Harmonized Standard, the reference of which will be published in the
Official Journal of the European Communities referencing the Directive 1999/5/EC [i.1] of the European Parliament
and of the Council of 9 March 1999 on radio equipment and telecommunications terminal equipment and the mutual
recognition of their conformity ("the R&TTE Directive") [i.1].
Technical specifications relevant to Directive 1999/5/EC [i.1] are given in annex A.
The present document is part 2 of a multi-part deliverable covering Short Range Devices (SRD); Ultra Low Power
Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to
405 MHz, as identified below:
Part 1: "Technical characteristics and test methods";
Part 2: "Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive".
National transposition dates
Date of adoption of this EN: 28 September 2009
Date of latest announcement of this EN (doa): 31 December 2009
Date of latest publication of new National Standard
or endorsement of this EN (dop/e): 30 June 2010
Date of withdrawal of any conflicting National Standard (dow): 30 June 2011
ETSI
6 ETSI EN 301 839-2 V1.3.1 (2009-10)
1 Scope
The present document applies to the following radio equipment types:
• Ultra Low Power Active Medical Implants (ULP-AMI);
• and Peripherals (ULP-AMI-P).
These radio equipment types are capable of operating in all or any part of the frequency bands in table 1.
Table 1: Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Transmit Ultra Low Power Active Medical Implants 402 MHz to 405 MHz
(ULP-AMI) and Peripherals (ULP-AMI-P)
Receive Ultra Low Power Active Medical Implants 402 MHz to 405 MHz
(ULP-AMI) and Peripherals (ULP-AMI-P)
The present document is intended to cover the provisions of Directive 1999/5/EC [i.1] (R&TTE Directive), Article 3.2,
which states that "…. radio equipment shall be so constructed that it effectively uses the spectrum allocated to
terrestrial/space radio communications and orbital resources so as to avoid harmful interference".
An AIMD is regulated under the AIMD Directive 90/385/EEC [i.2]: radio parts contained therein (referred to herein as
ULP-AMI and ULP-AMI-P for peripheral devices) are regulated under the Directive 1999/5/EC [i.1].
In addition to the present document, other ENs that specify technical requirements in respect of essential requirements
under other parts of Article 3 of the R&TTE Directive [i.1] may apply to equipment within the scope of the present
document.
NOTE: A list of such ENs is included on the web site http://www.newapproach.org.
2 References
References are either specific (identified by date of publication and/or edition number or version number) or
non-specific.
• For a specific reference, subsequent revisions do not apply.
• Non-specific reference may be made only to a complete document or a part thereof and only in the following
cases:
- if it is accepted that it will be possible to use all future changes of the referenced document for the
purposes of the referring document;
- for informative references.
Referenced documents which are not found to be publicly available in the expected location might be found at
http://docbox.etsi.org/Reference.
NOTE: While any hyperlinks included in this clause were valid at the time of publication ETSI cannot guarantee
their long term validity.
ETSI
7 ETSI EN 301 839-2 V1.3.1 (2009-10)
2.1 Normative references
The following referenced documents are indispensable for the application of the present document. For dated
references, only the edition cited applies. For non-specific references, the latest edition of the referenced document
(in
...
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Electromagnetic compatibility and Radio spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz - Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive33.100.01Elektromagnetna združljivost na splošnoElectromagnetic compatibility in general33.060.20Sprejemna in oddajna opremaReceiving and transmitting equipment11.040.40Implantanti za kirurgijo, protetiko in ortetikoImplants for surgery, prosthetics and orthoticsICS:Ta slovenski standard je istoveten z:EN 301 839-2 Version 1.3.1SIST EN 301 839-2 V1.3.1:2009en01-december-2009SIST EN 301 839-2 V1.3.1:2009SLOVENSKI
STANDARD
ETSI ETSI EN 301 839-2 V1.3.1 (2009-10) 2
Reference REN/ERM-TG30-263-2 Keywords radio, regulation, SRD, testing ETSI 650 Route des Lucioles F-06921 Sophia Antipolis Cedex - FRANCE
Tel.: +33 4 92 94 42 00
Fax: +33 4 93 65 47 16
Siret N° 348 623 562 00017 - NAF 742 C Association à but non lucratif enregistrée à la Sous-Préfecture de Grasse (06) N° 7803/88
Important notice Individual copies of the present document can be downloaded from: http://www.etsi.org The present document may be made available in more than one electronic version or in print. In any case of existing or perceived difference in contents between such versions, the reference version is the Portable Document Format (PDF). In case of dispute, the reference shall be the printing on ETSI printers of the PDF version kept on a specific network drive within ETSI Secretariat. Users of the present document should be aware that the document may be subject to revision or change of status. Information on the current status of this and other ETSI documents is available at http://portal.etsi.org/tb/status/status.asp If you find errors in the present document, please send your comment to one of the following services: http://portal.etsi.org/chaircor/ETSI_support.asp Copyright Notification No part may be reproduced except as authorized by written permission. The copyright and the foregoing restriction extend to reproduction in all media.
© European Telecommunications Standards Institute 2009. All rights reserved.
DECTTM, PLUGTESTSTM, UMTSTM, TIPHONTM, the TIPHON logo and the ETSI logo are Trade Marks of ETSI registered for the benefit of its Members. 3GPPTM is a Trade Mark of ETSI registered for the benefit of its Members and of the 3GPP Organizational Partners. LTE™ is a Trade Mark of ETSI currently being registered for the benefit of its Members and of the 3GPP Organizational Partners. GSM® and the GSM logo are Trade Marks registered and owned by the GSM Association. SIST EN 301 839-2 V1.3.1:2009
ETSI ETSI EN 301 839-2 V1.3.1 (2009-10) 3 Contents Intellectual Property Rights . 5 Foreword . 5 1 Scope . 6 2 References . 6 2.1 Normative references . 7 2.2 Informative references . 7 3 Definitions and abbreviations . 7 3.1 Definitions . 7 3.2 Abbreviations . 7 4 Technical requirements and specifications . 7 4.1 Environmental profile . 7 4.2 Conformance requirements . 8 4.2.1 Mechanical and electrical design . 8 4.2.1.1 General . 8 4.2.1.2 Antennas . 8 4.2.1.3 Controls . 8 4.2.1.4 Transmitter shut-off facility . 8 4.2.2 Frequency error . 8 4.2.2.1 Definition . 8 4.2.2.2 Limits . 8 4.2.2.3 Conformance . 8 4.2.3 Emission bandwidth . 8 4.2.3.1 Definition . 8 4.2.3.2 Limits . 8 4.2.3.3 Conformance . 8 4.2.4 Effective radiated power of the fundamental emission . 9 4.2.4.1 Definition . 9 4.2.4.2 Limits . 9 4.2.4.3 Conformance . 9 4.2.5 Spurious emissions of transmitter . 9 4.2.5.1 Definition . 9 4.2.5.2 Limits . 9 4.2.5.3 Conformance . 9 4.2.6 Frequency stability under low voltage conditions . 9 4.2.6.1 Definition . 9 4.2.6.2 Limits . 9 4.2.6.3 Conformance . 9 4.2.7 Spurious radiation of receivers . 9 4.2.7.1 Definition . 9 4.2.7.2 Limits . 9 4.2.7.3 Conformance . 9 4.2.8 Spectrum Access . 10 4.2.8.1 LBT/AFA spectrum access . 10 4.2.8.1.1 Definition. 10 4.2.8.1.2 Limits . 10 4.2.8.2 LP/LDC spectrum access . 10 4.2.8.2.1 Definition. 10 4.2.8.2.2 Limits . 10 4.2.8.3 Conformance . 10 5 Testing for compliance with technical requirements . 11 5.1 Environmental conditions for testing . 11 5.2 Interpretation of the measurement results . 11 5.3 Essential radio test suites . 11 SIST EN 301 839-2 V1.3.1:2009
ETSI ETSI EN 301 839-2 V1.3.1 (2009-10) 4 5.3.1 Frequency error . 11 5.3.2 Emission bandwidth . 12 5.3.3 Effective radiated power of the fundamental emission . 12 5.3.4 Spurious emissions of transmitter . 12 5.3.5 Frequency stability under low voltage conditions . 12 5.3.6 Spurious radiation of receivers . 12 5.3.7 Spectrum Access . 12 5.3.7.1 LBT/AFA spectrum access . 12 5.3.7.2 LP/LDC spectrum access . 12 5.3.8 Normal and extreme test-conditions . 12 5.3.9 Test power source . 12 5.3.10 Choice of samples for test suites . 12 Annex A (normative): HS Requirements and conformance Test specifications Table (HS-RTT) . 13 Annex B (informative): The EN title in the official languages . 15 Annex C (informative): Bibliography . 16 History . 17
ETSI ETSI EN 301 839-2 V1.3.1 (2009-10) 5 Intellectual Property Rights IPRs essential or potentially essential to the present document may have been declared to ETSI. The information pertaining to these essential IPRs, if any, is publicly available for ETSI members and non-members, and can be found in ETSI SR 000 314: "Intellectual Property Rights (IPRs); Essential, or potentially Essential, IPRs notified to ETSI in respect of ETSI standards", which is available from the ETSI Secretariat. Latest updates are available on the ETSI Web server (http://webapp.etsi.org/IPR/home.asp). Pursuant to the ETSI IPR Policy, no investigation, including IPR searches, has been carried out by ETSI. No guarantee can be given as to the existence of other IPRs not referenced in ETSI SR 000 314 (or the updates on the ETSI Web server) which are, or may be, or may become, essential to the present document. Foreword This Harmonized European Standard (Telecommunications series) has been produced by ETSI Technical Committee Electromagnetic compatibility and Radio spectrum Matters (ERM). The present document has been produced by ETSI in response to a mandate from the European Commission issued under Council Directive 98/34/EC (as amended) [i.3] laying down a procedure for the provision of information in the field of technical standards and regulations. The present document is intended to become a Harmonized Standard, the reference of which will be published in the Official Journal of the European Communities referencing the Directive 1999/5/EC [i.1] of the European Parliament and of the Council of 9 March 1999 on radio equipment and telecommunications terminal equipment and the mutual recognition of their conformity ("the R&TTE Directive") [i.1]. Technical specifications relevant to Directive 1999/5/EC [i.1] are given in annex A. The present document is part 2 of a multi-part deliverable covering Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz, as identified below: Part 1: "Technical characteristics and test methods"; Part 2: "Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive".
National transposition dates Date of adoption of this EN: 28 September 2009 Date of latest announcement of this EN (doa): 31 December 2009 Date of latest publication of new National Standard or endorsement of this EN (dop/e):
30 June 2010 Date of withdrawal of any conflicting National Standard (dow): 30 June 2011
ETSI ETSI EN 301 839-2 V1.3.1 (2009-10) 6 1 Scope The present document applies to the following radio equipment types: • Ultra Low Power Active Medical Implants (ULP-AMI); • and Peripherals (ULP-AMI-P). These radio equipment types are capable of operating in all or any part of the frequency bands in table 1. Table 1: Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) service frequency bands Transmit Ultra Low Power Active Medical Implants
(ULP-AMI) and Peripherals (ULP-AMI-P) 402 MHz to 405 MHz Receive Ultra Low Power Active Medical Implants
(ULP-AMI) and Peripherals (ULP-AMI-P) 402 MHz to 405 MHz
The present document is intended to cover the provisions of Directive 1999/5/EC [i.1] (R&TTE Directive), Article 3.2, which states that "…. radio equipment shall be so constructed that it effectively uses the spectrum allocated to terrestrial/space radio communications and orbital resources so as to avoid harmful interference". An AIMD is regulated under the AIMD Directive 90/385/EEC [i.2]: radio parts contained therein (referred to herein as ULP-AMI and ULP-AMI-P for peripheral devices) are regulated under the Directive 1999/5/EC [i.1]. In addition to the present document, other ENs that specify technical requirements in respect of essential requirements under other parts of Article 3 of the R&TTE Directive [i.1] may apply to equipment within the scope of the present document. NOTE: A list of such ENs is included on the web site http://www.newapproach.org. 2 References References are either specific (identified by date of publication and/or edition number or version number) or non-specific. • For a specific reference, subsequent revisions do not apply. • Non-specific reference may be made only to a complete document or a part thereof and only in the following cases: - if it is accepted that it will be possible to use all future changes of the referenced document for the purposes of the referring document; - for informative references. Referenced documents which are not found to be publicly
...