EN ISO 9626:1995/A1:2001
(Amendment)Stainless steel needle tubing for the manufacture of medical devices (ISO 9626:1991/AM 1:2001)
Stainless steel needle tubing for the manufacture of medical devices (ISO 9626:1991/AM 1:2001)
Migrated from Progress Sheet (TC Comment) (2000-07-10): Contact Mr Vyze ext 850 when processing this project through each stage
Edelstahlrohr zur Herstellung von Medizinprodukten (ISO 9626:1991/AM 1:2001)
Diese Internationale Norm beschreibt Maße und mechanische Eigenschaften von Edelstahlrohr mit normaler und dünner Rohrwand der nominalen metrischen Abmessungen von 3,4 mm bis 0,2 mm und von Rohren mit extra dünner Rohrwand der nominalen metrischen Abmessungen von 2,1 mm bis 0,6 mm.
Tubes d'aiguilles en acier inoxydable pour la fabrication de matériel médical (ISO 9626:1991/AM 1:2001)
Igle iz nerjavnega jekla za izdelavo medicinskih pripomočkov (ISO 9626:1991/AM1:2001)
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
01-maj-2002
,JOHL]QHUMDYQHJDMHNOD]DL]GHODYRPHGLFLQVNLKSULSRPRþNRY ,62
$0
Stainless steel needle tubing for the manufacture of medical devices (ISO 9626:1991/AM
1:2001)
Edelstahlrohr zur Herstellung von Medizinprodukten (ISO 9626:1991/AM 1:2001)
Tubes d'aiguilles en acier inoxydable pour la fabrication de matériel médical (ISO
9626:1991/AM 1:2001)
Ta slovenski standard je istoveten z: EN ISO 9626:1995/A1:2001
ICS:
11.040.25 Injekcijske brizge, igle in Syringes, needles an
katetri catheters
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
EUROPEAN STANDARD
EN ISO 9626:1995/A1
NORME EUROPÉENNE
EUROPÄISCHE NORM
June 2001
ICS 11.040.20
English version
Stainless steel needle tubing for the manufacture of medical
devices (ISO 9626:1991/AM 1:2001)
Tubes d'aiguilles en acier inoxydable pour la fabrication de Edelstahlrohr zur Herstellung von Medizinprodukten (ISO
matériel médical (ISO 9626:1991/AM 1:2001) 9626:1991/AM 1:2001)
This amendment A1 modifies the European Standard EN ISO 9626:1995; it was approved by CEN on 1 June 2001.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of this
amendment into the relevant national standard without any alteration. Up-to-date lists and bibliographical references concerning such
national standards may be obtained on application to the Management Centre or to any CEN member.
This amendment exists in three official versions (English, French, German). A version in any other language made by translation under the
responsibility of a CEN member into its own language and notified to the Management Centre has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece,
Iceland, Ireland, Italy, Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36 B-1050 Brussels
© 2001 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 9626:1995/A1:2001 E
worldwide for CEN national Members.
Page 2
Foreword
Corrected 2001-12-12
The text of this Amendment EN ISO 9626:1995/A1:2001 to the EN ISO 9626:1995 has
been prepared by Technical Committee ISO/TC 84 "Medical devices for injections" in
collaboration with Technical Committee CEN/TC 205 "Non-active medical devices", the
secretariat of which is held by BSI.
This European Standard shall be given the status of a national standard, either by
publication of an identical text or by endorsement, at the latest by December 2001, and
conflicting national standards shall be withdrawn at the latest by December 2001.
According to the CEN/CENELEC Internal Regulations, the national standards
organizations of the following countries are bound to implement this European Standard:
Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece,
Iceland, Ireland, Italy, Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden,
Switzerland and the United Kingdom.
Endorsement notice
The text of the Amendment to the International Standard ISO 9626:1991/AM 1:2001 has
been approved by CEN as an Amendment to the European Standard without any
modification.
NOTE Normative references to International Standards are listed in annex ZA (normative).
Page 3
Annex ZA
(normative)
Normative references to international publications with their relevant
European publications
This European Standard incorporates by dated or undated reference, provisions from other
publications. These normative references are cited at the appropriate places in the text and
the publications are listed hereafter. For dated references, subsequent amendments to or
revisions of any of these publications apply to this European Standard only when
incorporated in it by amendment or revision. For undated references the latest edition of
the publication referred to applies (including amendments).
NOTE Where an International Publication has been modified by common modifications, indicated by
(mod.), the relevant EN/HD applies.
Publication Year Title EN/HD Year
ISO 3696 1987 Water for analytical laboratory use - EN ISO 3696 1995
Specification and test methods
INTERNATIONAL ISO
STANDARD 9626
First edition
1991-09-01
AMENDMENT 1
2001-06-01
Stainless steel needle tubing for the
manufacture of medical devices —
AMENDMENT 1
Tubes d'aiguilles en acier inoxydable pour la fabrication de matériel
médical —
AMENDEMENT 1
Reference number
ISO 9626:1991/Amd.1:2001(E)
©
ISO 2001
ISO 9626:1991/Amd.1:2001(E)
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ii © ISO 2001 – All rights reserved
ISO 9626:1991/Amd.1:2001(E)
Foreword
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member bodies). The work of preparing International Standards is normally carried out through ISO technical
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