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SSH EN 868-7:2009

Materialet dhe sistemet e ambalazhmit për pajisjet mjekësore të cilat janë për t’u sterilizuar - Pjesa 7:Letër mbështjellëse adezive për prodhimin e pakove që mbyllen hermetikisht me nxehje për përdorim në mjekësi për sterilizimin me oksid etileni ose me

Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods
5 nën 2009
95.99 Withdrawal of Standard   23 tet 2017

General information

95.99     23 tet 2017

DPS

DPS/KT 206

European Norm

11.080.30  

anglisht  

Buying

Shfuqizuar

Language in which you want to receive the document.

Scope

paper complying with EN 868-6, used as sterile barrier systems and/or packaging systems that are intended
to maintain sterility of terminally sterilized medical devices to the point of use. The materials specified in this
part are intended to be used for ethylene oxide or irradiation sterilization.
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 or 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.

Related directives

Directives related to this standards.

93/42/EEC

Pajisje Mjekësore

2007/47/EC

Direktiva 2007/47/EC e Parlamentit Europian dhe e Këshillit të 5 shtator 2007 amendon Direktivën e Këshillit 90/385/EEC mbi përafrimin e ligjeve të Shteteve Anëtare në lidhje me pajisje medicinale aktive transplatuese, Direktiva e Këshillit 93/42/EEC në lidhje me pajisjet mjekësore dhe Direktivën 98/8/EC në lidhje me vendosjen e produkteve biocide në treg

Life cycle

NOW

WITHDRAWN
SSH EN 868-7:2009
95.99 Withdrawal of Standard
23 tet 2017

REVISED BY

WITHDRAWN
SSH EN 868-7:2005

PUBLISHED
SSH EN 868-7:2017

Related project

Adopted from EN 868-7:2009