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DIN EN 61326-2-6 : 2013

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - EMC REQUIREMENTS - PART 2-6: PARTICULAR REQUIREMENTS - IN VITRO DIAGNOSTIC (IVD) MEDICAL EQUIPMENT (IEC 61326-2-6:2012)

Superseded date

09-11-2022

Published date

12-01-2013

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DevelopmentNote
Supersedes DIN EN 61326. (10/2006) Supersedes DIN IEC 61326-2-6. (09/2013)
DocumentType
Standard
PublisherName
Verband Deutscher Elektrotechniker
Status
Superseded
SupersededBy
Supersedes

Standards Relationship
UNE-EN 61326-2-6:2006 Identical
EN 61326-2-6:2013 Identical
NBN EN 61326-2-6 : 2013 Identical
SN EN 61326-2-6 : 2006 Identical
VDE 0843-20-2-6 : 2013 Corresponds
IEC 61326-2-6:2012 Identical
NF EN 61326-2-6 : 2013 Identical
BS EN 61326-2-6:2013 Identical

DIN EN ISO 18113-3:2013-01 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
DIN EN ISO 18113-5:2013-01 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
DIN EN ISO 15197:2015-12 IN VITRO DIAGNOSTIC TEST SYSTEMS - REQUIREMENTS FOR BLOOD-GLUCOSE MONITORING SYSTEMS FOR SELF-TESTING IN MANAGING DIABETES MELLITUS (ISO 15197:2013)

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