BS EN ISO 8871-2:2004+A1:2014 - Elastomeric parts for parenterals and for devices for pharmaceutical use. Identification and characterization

BS EN ISO 8871-2:2004+A1:2014

Elastomeric parts for parenterals and for devices for pharmaceutical use. Identification and characterization

Status : Withdrawn   Published : September 2004 Replaced By : BS EN ISO 8871-2:2020

WITHDRAWN TITLE
*To ask about withdrawn titles contact the
Customer Relations
cservices@bsigroup.com, +44 345 086 9001





Standard NumberBS EN ISO 8871-2:2004+A1:2014
TitleElastomeric parts for parenterals and for devices for pharmaceutical use. Identification and characterization
StatusWithdrawn
Publication Date08 September 2004
Withdrawn Date08 June 2020
Normative References(Required to achieve compliance to this standard)ISO 2781:1988, ISO 48:1994, ISO 247:1990, ISO 8871-1:2003
Informative References(Provided for Information)ISO 8536-2:2001, ISO 9924-1:2000, ISO 3696:1987, ISO 8536-6:1995, ISO 8362-2:1988, ISO 11040-5:2001, ISO 8362-5:1995, ISO 815:1991, ISO 11040-2:1994
Replaced ByBS EN ISO 8871-2:2020
ReplacesBS EN ISO 8871:1997
International RelationshipsISO 8871-2:2003/Amd 1:2005,EN ISO 8871-2:2004/A1:2014
Amended ByAmendment, July 2014
DescriptorsDrug administration, Chemical analysis and testing, Drug containers, Natural rubber, Syringes, Elastomers, Physical property measurement, Determination of content, Injection instruments, Medical equipment, Drugs, Synthetic rubber, Identification methods, Parenteral infusion equipment
ICS11.040.20
Title in FrenchElements en elastomere pour administration parenteale et dispositifs a usage pharmaceutique. Identification et caracterisation
Title in GermanElastomere Teile fuer Parenteralia und fuer Produkte zur pharmazeutischen Verwendung. Identifizierung und Charakterisierung
CommitteeCH/212
ISBN978 0 580 84962 6
PublisherBSI
FormatA4
DeliveryYes
Pages34
File Size1.656 MB
Price£214.00


WITHDRAWN TITLE
*To ask about withdrawn titles contact the
Customer Relations
cservices@bsigroup.com, +44 345 086 9001
 Your basket
Your basket is empty

Multi-user access to over 3,500 medical device standards, regulations, expert commentaries and other documents


Develop a PAS

Develop a fast-track standardization document in 9-12 months


BSOL

The faster, easier way to work with standards


Worldwide Standards
We can source any standard from anywhere in the world