I.S. EN 556-2:2004
Superseded
View Superseded by
STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR MEDICAL DEVICES TO BE DESIGNATED 'STERILE' - PART 2: REQUIREMENTS FOR ASEPTICALLY PROCESSED MEDICAL DEVICES
Hardcopy , PDF
English
01-01-2004
10-09-2018
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
This European Standard specifies the requirements for an aseptically processed medical device
to be designated 'STERILE'.
| Committee |
TC 204
|
| DocumentType |
Standard
|
| Pages |
11
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| DIN EN 556-2:2004-03 | Equivalent |
| UNE-EN 556-2:2004 | Equivalent |
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