ONORM EN 556-1 : 2006
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR MEDICAL DEVICES TO BE DESIGNATED "STERILE" - PART 1: REQUIREMENTS FOR TERMINALLY STERILIZED MEDICAL DEVICES
08-26-2024
01-12-2013
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
Annex ZA (informative) - Clauses of this European
Standard addressing essential
requirements or other provisions
of EU Directives
Bibliography
Specifies the requirements for a terminally-sterilized medical device to be designated "STERILE".
| DocumentType |
Standard
|
| PublisherName |
Osterreichisches Normungsinstitut/Austrian Standards
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| DIN EN 556-1:2002-03 | Identical |
| EN 556-1:2001/AC:2006 | Identical |
| NS EN 556-1 : 2002 AC 2006 | Identical |
| UNE-EN 556-1:2002 | Identical |
| NBN EN 556-1 : 2001 COR 2006 | Identical |
| I.S. EN 556-1:2002 | Identical |
| UNI EN 556-1 : 2002 | Identical |
| BS EN 556-1:2001 | Identical |
| SN EN 556-1 : 2001 CORR 2006 | Identical |
| NF EN 556-1 : 2002 | Identical |
| NEN EN 556-1 : 2001 C1 2006 | Identical |
| ONORM EN ISO 5367 : 2015 | ANAESTHETIC AND RESPIRATORY EQUIPMENT - BREATHING SETS AND CONNECTORS (ISO 5367:2014) |
| EN ISO 13488 : 2000 | QUALITY SYSTEMS - MEDICAL DEVICES - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF EN ISO 9002 |
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