SIST EN 60601-1:1995/A2:1998
(Amendment)Medical electrical equipment -- Part 1: General requirements for safety
Medical electrical equipment -- Part 1: General requirements for safety
EN following parallel vote * Incorporates and supersedes A11 and A12
Medizinische elektrische Geräte -- Teil 1: Allgemeine Festlegungen für die Sicherheit
Appareils électromédicaux -- Partie 1: Règles générales de sécurité
Medical electrical equipment - Part 1: General requirements for safety - Amendment A2 (IEC 60601-1:1988/A2:1995 + ccorigendum jun. 1995)
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Standards Content (Sample)
SLOVENSKI SIST EN 60601-1:1995/A2:1998
prva izdaja
STANDARD
september 1998
Medical electrical equipment - Part 1: General requirements for safety -
Amendment A2 (IEC 60601-1:1988/A2:1995 + ccorigendum jun. 1995)
ICS 11.040.01 Referenčna šte
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Frequently Asked Questions
SIST EN 60601-1:1995/A2:1998 is a amendment published by the Slovenian Institute for Standardization (SIST). Its full title is "Medical electrical equipment -- Part 1: General requirements for safety". This standard covers: EN following parallel vote * Incorporates and supersedes A11 and A12
EN following parallel vote * Incorporates and supersedes A11 and A12
SIST EN 60601-1:1995/A2:1998 is classified under the following ICS (International Classification for Standards) categories: 11.040.01 - Medical equipment in general. The ICS classification helps identify the subject area and facilitates finding related standards.
SIST EN 60601-1:1995/A2:1998 has the following relationships with other standards: It is inter standard links to SIST EN 60601-1:2007, SIST EN 60601-1:1995. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
SIST EN 60601-1:1995/A2:1998 is associated with the following European legislation: EU Directives/Regulations: 90/385/EEC, 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.
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