Medical electrical equipment - Part 2-43: Particular requirements for the safety of X-ray equipment for interventional procedures

Establishes safety requirements for the design and manufacture of X-ray equipment for prolonged radioscopically guided interventional procedures. Specifies information which is to be provided with such equipment for the assistance of the user and operator in managing the radiation risk arising from these procedures which could affect patients and staff.

Medizinische elektrische Geräte - Teil 2-43: Besondere Festlegungen für die Sicherheit von Röntgeneinrichtungen für interventionelle Verfahren

Appareils électromédicaux - Partie 2-43: Règles particulières de sécurité pour les appareils radiologiques lors d'interventions

Medicinska električna oprema - 2-43. del: Posebne varnostne zahteve za rentgensko opremo za intervencijske postopke (IEC 60601-2-43:2000)

General Information

Status
Withdrawn
Publication Date
18-Dec-2000
Withdrawal Date
31-Jul-2003
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-Jun-2013
Completion Date
01-Jun-2013
Directive
Not Harmonized93/42/EEC - Medical devices
OJ Ref: C 173/2, C 293/39, C 293/39, C 293/39, C 293/39, C OJ Date: 24-Jan-2013

Relations

Effective Date
28-Jan-2023
Effective Date
03-Feb-2026
Effective Date
03-Feb-2026
Effective Date
03-Feb-2026
Effective Date
03-Feb-2026

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Standard

EN 60601-2-43:2002

English language (39 pages)
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Frequently Asked Questions

EN 60601-2-43:2000 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2-43: Particular requirements for the safety of X-ray equipment for interventional procedures". This standard covers: Establishes safety requirements for the design and manufacture of X-ray equipment for prolonged radioscopically guided interventional procedures. Specifies information which is to be provided with such equipment for the assistance of the user and operator in managing the radiation risk arising from these procedures which could affect patients and staff.

Establishes safety requirements for the design and manufacture of X-ray equipment for prolonged radioscopically guided interventional procedures. Specifies information which is to be provided with such equipment for the assistance of the user and operator in managing the radiation risk arising from these procedures which could affect patients and staff.

EN 60601-2-43:2000 is classified under the following ICS (International Classification for Standards) categories: 11.040.50 - Radiographic equipment. The ICS classification helps identify the subject area and facilitates finding related standards.

EN 60601-2-43:2000 has the following relationships with other standards: It is inter standard links to EN 60601-2-43:2010, EN 60601-2-28:1993, EN 60601-2-32:1994, HD 501 S1:1988, EN 60601-2-7:1998. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

EN 60601-2-43:2000 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 60601-2-43:2000 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 STANDARD
01-februar-2002
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Medical electrical equipment - Part 2-43: Particular requirements for the safety of X-ray
equipment for interventional procedures (IEC 60601-2-43:2000)
Medizinische elektrische Geräte - Teil 2-43: Besondere Festlegungen für die Sicherheit
von Röntgeneinrichtungen für interventionelle Verfahren (IEC 60601-2-43:2
...

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