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DIN EN 60601-1 VDE 0750-1 Berichtigung 1:2025-07

Medical electrical equipment

Part 1: General requirements for basic safety and essential performance

(IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); German version EN 60601-1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021; Corrigendum 1
Class/Status: Standard, valid
Released: 2025-07
VDE Art. No.: 0701614

Note: You can pre-order this document (delivery subject to availability). Valid from 2025-07-01.

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS.
The series does not apply to:
– in vitro diagnostic equipment that does not fall within the definition MEDICAL ELECTRICAL EQUIPMENT, for information, see IEC 61010 series;
– implantable parts of active implantable medical devices, for information, see ISO 14708 series;
– medical gas pipeline systems, for information, see ISO 7396-1.