BS EN 868-10:2009
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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Packaging for terminally sterilized medical devices Adhesive coated nonwoven materials of polyolefines. Requirements and test methods
Hardcopy , PDF
23-01-2019
English
31-10-2009
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Information to be supplied by the manufacturer
Annex A (informative) - Details of significant technical
changes between this European Standard
and the previous edition
Annex B (normative) - Method for the determination of mass
per unit area of uncoated nonwoven
polyolefine materials and adhesive coating
Annex C (normative) - Method for the determination of the
seal strength and visual inspection of the
adhesive coating
Bibliography
Gives test methods and values for sealable adhesive coated nonwoven materials of polyolefines, manufactured from nonwovens complying with EN 868-9 used for sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use.
Committee |
CH/198
|
DevelopmentNote |
Supersedes 98/122772 DC. (05/2005) Supersedes 07/30167336 DC. (10/2009)
|
DocumentType |
Standard
|
Pages |
16
|
PublisherName |
British Standards Institution
|
Status |
Withdrawn
|
SupersededBy | |
Supersedes |
polyolefines, manufactured from nonwovens complying with EN 868-9 used for sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use. NOTE 1 The need for a protective packaging may be determined by the manufacturer and the user. This part of EN 868 only introduces performance requirements and test methods that are specific to the products covered by this part of EN 868 but does not add nor modify the general requirements specified in EN ISO 11607-1. As such, the particular requirements in 4.2 to 4.3 can be used to demonstrate compliance with one or more but not all of the requirements of EN ISO 11607-1. NOTE 2 When additional materials are used inside the sterile barrier system in order to ease the organization, drying or aseptic presentation (e.g. inner wrap, container filter, indicators, packing lists, mats, instrument organizer sets, tray liners or an additional envelope around the medical device) then other requirements, including the determination of the acceptability of these materials during validation activities, may apply. The materials specified in this part of EN 868 are intended for single use only.
Standards | Relationship |
NS EN 868-10 : 2009 | Identical |
NBN EN 868-10 : 2009 | Identical |
DIN EN 868-10:2009-09 | Identical |
UNI EN 868-10 : 2009 | Identical |
ONORM EN 868-10 : 2009 | Identical |
SN EN 868-10 : 2009 | Identical |
I.S. EN 868-10:2009 | Identical |
NEN EN 868-10 : 2009 | Identical |
NF EN 868-10 : 2009 | Identical |
UNE-EN 868-10:2009 | Identical |
EN 868-10:2009 | Identical |
ISO 1974:2012 | Paper — Determination of tearing resistance — Elmendorf method |
ISO 5636-3:2013 | Paper and board — Determination of air permeance (medium range) — Part 3: Bendtsen method |
ISO 11607-2:2006 | Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes |
EN 20811:1992 | Textiles - Determination of resistance to water penetration - Hydrostatic pressure test |
ISO 6588-2:2012 | Paper, board and pulps Determination of pH of aqueous extracts Part 2: Hot extraction |
EN 21974:1994 | Paper - Determination of tearing resistance (Elmendorf method) (ISO 1974:1990) |
ISO 2758:2014 | Paper Determination of bursting strength |
EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
EN ISO 1924-2:2008 | Paper and board - Determination of tensile properties - Part 2: Constant rate of elongation method (20 mm/min) (ISO 1924-2:2008) |
EN ISO 536:2012 | Paper and board - Determination of grammage (ISO 536:2012) |
ISO 8601:2004 | Data elements and interchange formats Information interchange Representation of dates and times |
ISO 1924-2:2008 | Paper and board — Determination of tensile properties — Part 2: Constant rate of elongation method (20 mm/min) |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 536:2012 | Paper and board Determination of grammage |
EN ISO 2758:2014 | Paper - Determination of bursting strength (ISO 2758:2014) |
ISO 11607-1:2006 | Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems |
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