EN 60601-2-37:2001
(Main)Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Establishes particular requirements for the safety of ultrasonic diagnostic equipment and those aspects thereof which are directly related to safety. Does not cover ultrasonic therapeutic equipment; however, equipment used for the imaging of body structures by ultrasound in conjunction with therapeutic modalities is covered.
Medizinische elektrische Geräte - Teil 2-37: Besondere Festlegungen für die Sicherheit von Ultraschall-Geräten für die medizinische Diagnose und Überwachung
Appareils électromédicaux - Partie 2-37: Règles particulières de sécurité pour les appareils de diagnostic et de surveillance médicaux à ultrasons
Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment (IEC 60601-2-37:2001)
General Information
- Status
- Withdrawn
- Publication Date
- 16-Oct-2001
- Withdrawal Date
- 30-Sep-2004
- Technical Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Drafting Committee
- IEC/SC 62B - IEC_SC_62B
- Parallel Committee
- IEC/SC 62B - IEC_SC_62B
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 01-Oct-2010
- Completion Date
- 01-Oct-2010
Relations
- Effective Date
- 28-Jan-2023
- Effective Date
- 29-Jan-2023
- Effective Date
- 28-Jan-2023
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Frequently Asked Questions
EN 60601-2-37:2001 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment". This standard covers: Establishes particular requirements for the safety of ultrasonic diagnostic equipment and those aspects thereof which are directly related to safety. Does not cover ultrasonic therapeutic equipment; however, equipment used for the imaging of body structures by ultrasound in conjunction with therapeutic modalities is covered.
Establishes particular requirements for the safety of ultrasonic diagnostic equipment and those aspects thereof which are directly related to safety. Does not cover ultrasonic therapeutic equipment; however, equipment used for the imaging of body structures by ultrasound in conjunction with therapeutic modalities is covered.
EN 60601-2-37:2001 is classified under the following ICS (International Classification for Standards) categories: 11.040.55 - Diagnostic equipment; 17.140.50 - Electroacoustics. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-37:2001 has the following relationships with other standards: It is inter standard links to EN 60601-2-37:2008, EN 60601-2-37:2001/A1:2005, EN 60601-2-37:2001/A2:2005. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-37:2001 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/023, M/432. 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.
EN 60601-2-37:2001 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)
SLOVENSKI SIST EN 60601-2-37:2002
prva izdaja
STANDARD
junij 2002
Medical electrical equipment - Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment (IEC 60601-2-37:2001)
ICS 11.040.55; 17.140.50 Referenčna številka
© Standard je založil in izdal Slovenski inštitut za standardizacijo. Razmnoževanje ali kopiranje celote ali delov tega dokumenta ni dovoljeno
EUROPEAN STANDARD EN 60601-2-37
NORME EUROPÉENNE
EUROPÄISCHE NORM October 2001
ICS 11.040.55; 17.140.50
English version
Medical electrical equipment
Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment
(IEC 60601-2-37:2001)
Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-37: Règles particulières de Teil 2-37: Besondere Festlegungen für
sécurité pour les appareils de diagnostic die Sicherheit von Ultraschall-Geräten
et de surveillance médicaux à ultrasons für die medizinische Diagnose und
(CEI 60601-2-37:2001) Überwachung
(IEC 60601-2-37:2001)
This European Standard was approved by CENELEC on 2001-09-25. CENELEC members are bound to
comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration.
Up-to-date lists and bibliographical references concerning such national standards may be obtained on
application to the Central Secretariat or to any CENELEC member.
This European Standard exists in three official versions (English, French, German). A version in any other
language made by translation under the responsibility of a CENELEC member into its own language and
notified to the Central Secretariat has the same status as the official versions.
CENELEC members are the national electrotechnical committees of Austria, Belgium, Czech Republic,
Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembo
...
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