Medical electrical equipment - Part 2: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient, the operator, staff associated with magnetic resonance equipment and the general public. It also provides methods for demonstrating compliance with those requirements.

Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von medizinischen diagnostischen Magnetresonanzgeräten

Appareils électromédicaux - Partie 2: Règles particulières de sécurité relatives aux appareils à résonance magnétique pour diagnostic médical

Fixe les règles de sécurité relatives aux appareils à résonance magnétique, en vue d'assurer la protection du patient, de l'opérateur, du personnel associé aux appareils à résonance magnétique et du public en général, et propose des méthodes de démonstration de conformité avec les règles susdites.

Medical electrical equipment - Part 2: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:1995)

General Information

Status
Withdrawn
Publication Date
26-Nov-1995
Withdrawal Date
30-Jun-1996
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-Jul-2005
Completion Date
01-Jul-2005

Relations

Effective Date
28-Jan-2023
Effective Date
29-Jan-2023
Standard

EN 60601-2-33:1998

English language
61 pages
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Frequently Asked Questions

EN 60601-2-33:1995 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis". This standard covers: Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient, the operator, staff associated with magnetic resonance equipment and the general public. It also provides methods for demonstrating compliance with those requirements.

Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient, the operator, staff associated with magnetic resonance equipment and the general public. It also provides methods for demonstrating compliance with those requirements.

EN 60601-2-33:1995 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 60601-2-33:1995 has the following relationships with other standards: It is inter standard links to EN 60601-2-33:2002, EN 60601-2-33:1995/A11:1997. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

EN 60601-2-33:1995 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/023. 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 60601-2-33:1995 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 60601-2-33:1998
prva izdaja
STANDARD
september 1998
Medical electrical equipment - Part 2: Particular requirements for the safety of
magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:1995)
ICS 11.040.50 Refere
...

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