NEN-EN-ISO 15225/A2
Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange
inactive
| Organization: | NEN |
| Publication Date: | 1 April 2006 |
| Status: | inactive |
| Page Count: | 6 |
| ICS Code (IT applications in health care technology): | 35.240.80 |
| ICS Code (Medical equipment in general): | 11.040.01 |
scope:
add Annex ZC (informative) for relationship with directive 98/79/EC
Document History
April 1, 2016
Medical devices - Quality management - Medical device nomenclature data structure
NEN-EN- ISO 15225 specifies rules and guidelines for a medical device nomenclature data structure, in order to facilitate cooperation and exchange of data used by regulatory bodies on an...
May 1, 2010
Medical devices - Quality management - Medical device nomenclature data structure
This International Standard provides rules and guidelines for a medical device nomenclature data structure, in order to facilitate cooperation and exchange of data used by regulatory bodies on an...
April 1, 2008
Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange
This International Standard provides rules and guidelines for a medical device nomenclature data structure in order to facilitate cooperation and exchange of data used by regulatory bodies on an...
NEN-EN-ISO 15225/A2
April 1, 2006
Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange
add Annex ZC (informative) for relationship with directive 98/79/EC
February 1, 2004
Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange
A description is not available for this item.
March 1, 2002
Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange
A description is not available for this item.
December 1, 2000
Nomenclature - Specification for a nomenclature system for medical devices for the purposes of regulatory data exchange
Specifies requirements and guidance for the construction of a nomenclature for medical devices in order to facilitate co-operation and exchange of regulatory data on an international level between...