发布时间：2024-05-27 17:49:26 - 更新时间：2024年06月29日 15:22
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This part of ISO 8871 specifies evaluation procedures applicable to elastomeric parts used for drug containers and medical devices in order
Elastomeric parts for parenterals and for devices for pharmaceutical use - Identification and characterization
1. Diese Norm befa?t sich mit elastomeren Teilen bei Prim?rpackmitteln und medizinischen Ausstattungen, die in direktem Kontakt mit w??rigen
Elastomeric parts for aqueous parenteral preparations (ISO 8871:1988)
Elastomeric parts for aqueous parenteral preparations (ISO 8871:1988)
Elastomeric parts for aqueous parenteral preparations (ISO 8871: 1988)
Elastomeric Parts for Aqueous Parenteral Preparations
Elastomeric parts for aqueous parenteral preparations; Amendment 1
Elastomeric parts for parenterals and for devices for pharmaceutical use. Functional requirements and testing
1 This part of ISO 8871 defines procedures for classifying elastomeric parts for primary packs and medical devices used in direct contact
Elastomeric parts for parenterals and for devices for pharmaceutical use - Extractables in aqueous autoclavates
1 This International Standard defines procedures for identifying and classifying elastomeric parts for primary packs and medical devices used
Elastomeric parts for aqueous parenteral preparations
This document specifies identification and characterization procedures applicable to elastomeric parts including coated stoppers used for drug
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2020)
This part of ISO 8871 specifies evaluation procedures applicable to elastomeric parts used for drug containers and medical devices in order
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2 : identification and characterization.
이 표준은 (적합성 평가) 승인 절차 과정에서 평가한 표본과 현재 공급품 사이의 제품 동질
Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 2：Identification and characterization
Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 2：Identification and characterization
The project specifies evaluation procedures applicable to elastomeric parts used for drug containers and medical devices in order to guarantee
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003); German version EN ISO 8871-2:2004, text in German and English
This part of ISO 8871 specifies evaluation procedures applicable to elastomeric parts used for drug containers and medical devices in order
Elastomeric parts for parenterals and for devices for pharmaceutical use - Identification and characterization
1. Diese Norm befa?t sich mit elastomeren Teilen bei Prim?rpackmitteln und medizinischen Ausstattungen, die in direktem Kontakt mit w??rigen
Elastomeric parts for aqueous parenteral preparations (ISO 8871:1988)
Elastomeric parts for aqueous parenteral preparations (ISO 8871:1988)
Elastomeric parts for aqueous parenteral preparations (ISO 8871: 1988)
Elastomeric Parts for Aqueous Parenteral Preparations
Elastomeric parts for aqueous parenteral preparations; Amendment 1
Elastomeric parts for parenterals and for devices for pharmaceutical use. Functional requirements and testing
1 This part of ISO 8871 defines procedures for classifying elastomeric parts for primary packs and medical devices used in direct contact
Elastomeric parts for parenterals and for devices for pharmaceutical use - Extractables in aqueous autoclavates
1 This International Standard defines procedures for identifying and classifying elastomeric parts for primary packs and medical devices used
Elastomeric parts for aqueous parenteral preparations
This document specifies identification and characterization procedures applicable to elastomeric parts including coated stoppers used for drug
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2020)
This part of ISO 8871 specifies evaluation procedures applicable to elastomeric parts used for drug containers and medical devices in order
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2 : identification and characterization.
이 표준은 (적합성 평가) 승인 절차 과정에서 평가한 표본과 현재 공급품 사이의 제품 동질
Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 2：Identification and characterization
Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 2：Identification and characterization
The project specifies evaluation procedures applicable to elastomeric parts used for drug containers and medical devices in order to guarantee
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003); German version EN ISO 8871-2:2004, text in German and English
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