NS EN 1041 : 2008 + A1 2013
Current
Current
The latest, up-to-date edition.
INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES
Published date
12-01-2013
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Defines requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical devices and Council Directive 93/42/EEC concerning medical devices.
| DevelopmentNote |
2008 Edition Re-Issued in December 2013 and incorporates AMD 1 2013. (12/2013)
|
| DocumentType |
Standard
|
| PublisherName |
Norwegian Standards (Norges Standardiseringsforbund)
|
| Status |
Current
|
| Standards | Relationship |
| I.S. EN 1041:2008+A1:2013 | Identical |
| EN 1041:2008+A1:2013 | Identical |
| DIN EN 1041:2013-12 | Identical |
| UNE-EN 1041:2009 | Identical |
| BS EN 1041 : 2008 | Identical |
Summarise
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