NBN EN 868-2 : 2009
Current
The latest, up-to-date edition.
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: STERILIZATION WRAP - REQUIREMENTS AND TEST METHODS
01-12-2013
Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
4 Requirements
Annex A (normative) Method for the determination of
repellency to low surface
tension liquids
Annex B (normative) Method for the determination of
water repellency
Annex C (normative) Method for the determination of
pore size
Annex D (normative) Method for the determination of
drape
Annex E (normative) Method for the determination of
saline repellency
Annex F (normative) Method for the determination of
air penetration - porosity
Annex G (informative) Dimensions and tolerances
Gives examples of particular requirements and test procedures for sterilization wrap suitable to use as packaging for medical devices which are to be terminally sterilized.
DocumentType |
Standard
|
PublisherName |
Belgian Standards
|
Status |
Current
|
Standards | Relationship |
UNE-EN 868-2:2017 | Identical |
UNI EN 868-2 : 2009 | Identical |
EN 868-2:2017 | Identical |
SN EN 868-2:2017 | Identical |
DIN EN 868-2:2017-05 | Identical |
DIN EN 868-2:2015-08 (Draft) | Identical |
BS EN 868-2:2017 | Identical |
I.S. EN 868-2:2017 | Identical |
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