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CEN - EN 376

Information Supplied by the Manufacturer with in Vitro Diagnostic Reagents for Self-Testing

inactive, Most Current
Organization: CEN
Publication Date: 1 February 2002
Status: inactive
Page Count: 18
ICS Code (Laboratory medicine): 11.100

Document History

EN 376
February 1, 2002
Information Supplied by the Manufacturer with in Vitro Diagnostic Reagents for Self-Testing
A description is not available for this item.
EN 376
May 1, 1992
In Vitro Diagnostic Systems - Requirements for Labelling of In Vitro Diagnostic Reagents for Self-Testing
A description is not available for this item.

References

This document is referenced by:
ISO 19001 - In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
Published by ISO on March 15, 2013
This International Standard specifies requirements for information supplied by the manufacturer with reagents used in staining in biology. It applies to producers, suppliers and vendors of dyes,...
This document is referenced by:
SN EN ISO 18113-1 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
Published by SNV on May 1, 2012
This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This part of ISO...
This document is referenced by:
EN 980 - Symbols for use in the labelling of medical devices
Published by CEN on May 1, 2008
This European Standard specifies symbols for use in the information supplied by the manufacturer with medical devices. The requirements of this European Standard are not intended to apply to symbols...
This document is referenced by:
SN EN ISO 15197 - In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
Published by SNV on November 1, 2015
A description is not available for this item.
This document is referenced by:
EN 1041 - Information supplied by the manufacturer of medical devices
Published by CEN on August 1, 2008
This European Standard specifies requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical...
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