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CEN - EN 592

Instructions for Use in Vitro Diagnostic Instruments for Self-Testing

inactive, Most Current
Organization: CEN
Publication Date: 1 February 2002
Status: inactive
Page Count: 14
ICS Code (Laboratory medicine): 11.100

Document History

EN 592
February 1, 2002
Instructions for Use in Vitro Diagnostic Instruments for Self-Testing
A description is not available for this item.
EN 592
September 1, 1994
In Vitro Diagnostic Systems - Requirements for User Manuals for In Vitro Diagnostic Instruments for Home Use
A description is not available for this item.

References

This document is referenced by:
SN EN ISO 18113-5 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
Published by SNV on May 1, 2012
This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD instruments for self-testing. This part of ISO 18113 also applies to apparatus and equipment intended...
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...
This document is referenced by:
CEI UNI EN 1041 - Information supplied by the manufacturer of medical devices
Published by CEI on April 1, 2014
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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