NEN EN ISO 14160 : 2011
Current
The latest, up-to-date edition.
STERILIZATION OF HEALTH CARE PRODUCTS - LIQUID CHEMICAL STERILIZING AGENTS FOR SINGLE-USE MEDICAL DEVICES UTILIZING ANIMAL TISSUES AND THEIR DERIVATIVES - REQUIREMENTS FOR CHARACTERIZATION, DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES
12-01-2013
1 Scope
2 Normative references
3 Definitions
4 General
5 Validation
6 Process control and monitoring
7 Product release from sterilization
Annexes
A Guidance
B References to European Standards with their relevant
equivalents
C Bibliography
Defines requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization by liquid chemical sterilizing agents of single-use medical devices comprising, in whole or in part, materials of animal origin.
| DocumentType |
Standard
|
| PublisherName |
Netherlands Standards
|
| Status |
Current
|
| Standards | Relationship |
| ONORM EN ISO 14160 : 2011 | Identical |
| ISO 14160:2011 | Identical |
| I.S. EN ISO 14160:2011 | Identical |
| UNI EN ISO 14160 : 2011 | Identical |
| BS EN ISO 14160:2011 | Identical |
| SN EN ISO 14160 : 2011 | Identical |
| NF EN ISO 14160 : 2011 | Identical |
| DIN EN ISO 14160:2011-10 | Identical |
| UNE-EN ISO 14160:2012 | Identical |
| EN ISO 14160:2011 | Identical |
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