This site uses cookies and visit counters for operation and statistics. Privacy policy
Found: 60+
Overview EN ISO 8871-5:2025 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing - is the CEN-adopted version of ISO 8871-5:2025. I…
Overview EN ISO 8872:2022 - titled Aluminium caps and aluminium/plastic caps for infusion bottles and injection vials - General requirements and test methods - is a harmonized European adoption of IS…
Overview EN ISO 8871-2:2020 - "Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization" (ISO 8871-2:2020) specifies procedures for the i…
Overview SIST EN ISO 8871-3:2004/A1:2019 is a European amendment to the international standard ISO 8871-3:2003/Amd 1:2018. It focuses on elastomeric parts used in parenteral and pharmaceutical device…
Overview EN ISO 8871-3:2004/A1:2019 is a European amendment to the international standard ISO 8871-3:2003/Amd 1:2018. It focuses on elastomeric parts used in parenteral and pharmaceutical devices, sp…
Overview ISO 8873-2:2007 - Rigid cellular plastics: Spray-applied polyurethane foam for thermal insulation - Part 2: Application defines requirements for the application and installation of spray-app…
Overview ISO 8873-3:2007 - “Rigid cellular plastics - Spray-applied polyurethane foam for thermal insulation - Part 3: Test methods” defines the laboratory test procedures used to verify spray‑applie…
Overview ISO 8873-1:2006 - "Rigid cellular plastics - Spray-applied polyurethane foam for thermal insulation - Part 1: Material specifications" defines minimum material requirements and test methods…
Overview EN ISO 8871-4:2006 - "Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods" (ISO 8871-4:2006) specifies biological safe…
Overview EN ISO 8871-1:2004 (ISO 8871-1:2003) specifies chemical test methods to classify and evaluate elastomeric parts for parenterals and pharmaceutical devices by determining extractables in aque…
Overview SIST EN ISO 8871-3:2004 is a critical international standard developed by CEN and ISO that specifies methods for evaluating elastomeric parts used in parenteral and pharmaceutical devices. S…
Overview EN ISO 8871-3:2004 is a critical international standard developed by CEN and ISO that specifies methods for evaluating elastomeric parts used in parenteral and pharmaceutical devices. Specif…
Overview EN ISO 887:2000 (ISO 887:2000) - "Plain washers for metric bolts, screws and nuts for general purposes - General plan" - defines the general dimensional system and preferred combinations for…
Overview ISO 8871-3:2003/Amd 1:2018 is an essential international standard concerning elastomeric parts used in parenteral and pharmaceutical devices. This document is an amendment to Part 3 of ISO 8…
Overview ISO 8879:1986/Cor 2:1999 is Technical Corrigendum 2 to the original ISO 8879 standard for the Standard Generalized Markup Language (SGML). Published in 1999, this corrigendum corrects termin…
Overview ISO 8879:1986/Amd 1:1988 is Amendment 1 to ISO 8879:1986 - the international standard for the Standard Generalized Markup Language (SGML). Published by ISO in 1988, this amendment enhances t…
What is ISO 8871-2 about? ISO 8871 discusses elastomeric parts for parenterals and for devices for pharmaceutical use. ISO 8871-2 layouts identification and characterization procedures applicable to…
1 Scope This International Standard specifies general requirements and test methods for aluminium caps for injection vials, and for infusion and transfusion bottles.
1 Scope This International Standard specifies the full range of the nominal dimensions of product-grade-A and -C plain washers for general-purpose bolts, screws and nuts of nominal thread diameters r…
Overview ISO 8871-2:2020 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization - sets out identification and characterization proced…
Overview ISO 8871-1:2003 - “Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 1: Extractables in aqueous autoclavates” defines chemical evaluation procedures for elastom…
Overview ISO 8871-5:2025 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing defines functional requirements and test methods for…
Overview ISO 8870:2006 (IDF 83:2006) - "Milk and milk‑based products - Detection of thermonuclease produced by coagulase‑positive staphylococci" specifies a microbiological method for detecting heat‑…
Overview ISO 8871-3:2003 specifies laboratory methods to determine the number of visible and subvisible particles released from elastomeric parts used with parenterals and pharmaceutical devices. The…
Overview ISO 8872:2022 specifies general requirements and test methods for aluminium caps and aluminium/plastic caps used on infusion bottles and injection vials. This third edition (2022) integrates…
Overview ISO 8879:1986 - Standard Generalized Markup Language (SGML) - is the International Standard for defining and encoding the logical structure of text and office documents. Published by ISO for…
1 Scope 1.1 This part of ISO 8871 defines procedures for classifying elastomeric parts for primary packs and medical devices used in direct contact with preparations for parenteral use, including bot…
