EN 60601-2-33:2002
(Main)Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
General Information
- Abstract
Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient. Establishes requirements to provide information to the operator, staff associated with magnetic resonance equipment and the general public. Provides methods for demonstrating compliance with those requirements.
- Status
- Withdrawn
- Publication Date
- 07-Oct-2002
- Withdrawal Date
- 30-Jun-2005
- 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-2013
- Completion Date
- 01-Oct-2013
- Directive
- Not Harmonized93/42/EEC - Medical devicesOJ Ref: C, C 173/2, C 293/39, C 22/02 OJ Date: 24-Jan-2013
Relations
- Effective Date
- 28-Jan-2023
- Effective Date
- 28-Jan-2023
- Effective Date
- 28-Jan-2023
- Effective Date
- 10-Feb-2026
- Effective Date
- 10-Feb-2026
- Effective Date
- 09-Feb-2026
- Effective Date
- 09-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 03-Feb-2026
- Effective Date
- 29-Jan-2023
- Effective Date
- 29-Jan-2023
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Frequently Asked Questions
EN 60601-2-33:2002 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2-33: 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. Establishes requirements to provide information to the operator, staff associated with magnetic resonance equipment and the general public. Provides methods for demonstrating compliance with those requirements.
Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient. Establishes requirements to provide information to the operator, staff associated with magnetic resonance equipment and the general public. Provides methods for demonstrating compliance with those requirements.
EN 60601-2-33:2002 is classified under the following ICS (International Classification for Standards) categories: 11.040.55 - Diagnostic equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-33:2002 has the following relationships with other standards: It is inter standard links to EN 60601-2-33:1995/A11:1997, EN 60601-2-33:1995, EN 60601-2-33:2010, ISO 1999:1990, ISO 3864:1984, EN 1060-1:1995/A1:2002, EN 457:1992, EN 60651:1994/A1:1994, EN 60601-1-2:2001, HD 501 S1:1988, EN 60804:2000, EN 60651:1994/A2:2001, EN 60651:1994, EN 60601-2-33:2002/A2:2008, EN 60601-2-33:2002/A1:2005. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-33:2002 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: 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 60601-2-33:2002 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)
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Medical electrical equipment - Part 2-33: Particular requirements for the safety of
magnetic resonance equipment for medical diagnosis (IEC 60601-2- 33:2002)
Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit
von Magnetresonanzgerä
...