DIN EN ISO 23640:2015
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2015
- Standard No.
- DIN EN ISO 23640:2015
- Release Date
- 2015
- Published By
- German Institute for Standardization
- Status
- Replace By
- DIN EN ISO 23640:2015-12
- Latest
- DIN EN ISO 23640:2015-12
- Replace
- DIN EN ISO 23640:2013
DIN EN ISO 23640:2015 Referenced Document
- CLSI EP25-A-2009
- DIN EN ISO 14971:2013 Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01); German version EN ISO 14971:2012
- EN 13640:2002 Stability Testing of in Vitro Diagnostic Reagents
- ISO 14971:2007 Medical devices - Application of risk management to medical devices
- ISO 18113-1:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
DIN EN ISO 23640:2015 history
- 2015 DIN EN ISO 23640:2015-12 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2015 / Note: DIN EN ISO 23640 (2013-09) remains valid alongside this standard until 2018-06-30.
- 2015 DIN EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2015
- 2013 DIN EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2013
- 2012 DIN EN ISO 23640:2012 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2011
