SN EN ISO 11137-1 : 2015
Current
Current
The latest, up-to-date edition.
STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11137-1:2006, INCLUDING AMD 1:2013)
Available format(s)
Hardcopy
Published date
01-12-2015
Publisher
Important note : Users cannot be edited or removed once added to your Multi user PDF.ISO 11137-1:2006 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
| Committee |
INB/NK 171
|
| DevelopmentNote |
Supersedes SN EN 552. (07/2006)
|
| DocumentType |
Standard
|
| Pages |
0
|
| PublisherName |
Swiss Standards
|
| Status |
Current
|
| Standards | Relationship |
| NBN EN ISO 11137-1 : 2015 | Identical |
| NEN EN ISO 11137-1 : 2015 | Identical |
| EN ISO 11137-1:2015 | Identical |
| DIN EN ISO 11137-1:2015-11 | Identical |
| ISO 11137-1:2006 | Identical |
| BS EN ISO 11137-1:2015 | Identical |
| UNI EN ISO 11137-1 : 2013 | Identical |
| NF EN ISO 11137-1 : 2016 | Identical |
| NS EN ISO 11137-1 : 2015 | Identical |
| UNE-EN ISO 11137-1:2015 | Identical |
| I.S. EN ISO 11137-1:2015 | Identical |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.