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ISO 595-1 - Reusable All-Glass or Metal-and-Glass Syringes for Medical Use - Part 1: Dimensions
January 1, 1986 - ISO

Scope and field of application This part of ISO 595 specifies dimensions for reusable all-glass or metal-and-glass syringes for medical use, having a graduated capacity from 1 to 100 ml. lt also specifies requirements for the graduated capacity of syringes. ISO 595/2 specifies...

BS 1263-1 - Reusable hypodermic syringes for medical use - Part 1: Specification for dimensions of all-glass and metal-and-glass syringes
January 31, 1990 - BSI

Dimensions and graduated capacities for syringes having a graduated capacity from 1 mL to 100 mL.

BS EN ISO 595-2 - Reusable all-glass or metal-and-glass syringes for medical use - Part 2: Design, performance requirements and tests
January 31, 1990 - BSI

Design, performance and corresponding test methods for syringes having a graduated capacity from 1 ml to 100 ml.

DIN 13099 - Disposahle plastic syringes for medical use - Ttesting of the interaction between syringes and pharmaceutical preparation
October 1, 1970 - DIN

Geltungsbereich und Zweck Diese Norm gilt für die Anwendung von Injektionslösungen mit Einmalspritzen aus Kunststoffen nach DIN 13 098 (Vornorm). Nach DIN 13 098 (Vornorm), Ausgabe Oktober 1970, Abschnitt 2.3.4, Abschnitt 9.2 und dazugehörigen Prüfungen wird ausgeschlossen, daß Kunststoff und...

DS/ISO 594-1 - Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment – Part 1: General requirements
April 14, 1988 - DS

This part of DS/ISO 594 specifies requirements for conical fittings with a 6% Luer taper for use with hypodermic syringes and needles and with certain other apparatus for medical use such as tranfusion and infusion sets.

DS/EN 1707 - Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment – Lock fittings
February 18, 1997 - DS

The standard specifies requirements for conical lock fittings with 6% (Luer) taper for use with hypodermic syringes and needles and with certain other apparatus for medical use e.g. transfusion equipment. The requirements apply to fittings made of rigid and of semi-rigid materials and...

ISO 594-2 - Conical Fittings with a 6 % (Luer) Taper for Syringes, Needles and Certain Other Medical Equipment - Part 2: Lock Fittings
September 1, 1998 - ISO

This part of ISO 594 specifies requirements for conical lock fittings with a 6 % (Luer) taper for use with hypodermic syringes and needles and with certain other apparatus for medical use, e.g. transfusion equipment. The requirements apply to fittings made of rigid and of semi-rigid...

ISO 594-1 - Conical Fittings with a 6 % (Luer) Taper for Syringes, Needles and Certain Other Medical Equipment - Part 1: General Requirements
January 1, 1986 - ISO

Scope and field of application This part of ISO 594 specifies requirements for conical fittings with a 6 % (Luer) taper for use with hypodermic syringes and needles and with certain other apparatus for medical use such as transfusion and infusion sets. It covers conical fittings made...

JIS T 3224 - Sterile syringe filter
March 1, 2021 - JSA
A description is not available for this item.
ISO 7886-2 - Sterile hypodermic syringes for single use — Part 2: Syringes for use with power-driven syringe pumps
April 1, 2020 - ISO

This document specifies requirements for sterile single-use hypodermic syringes of nominal capacity 1 ml and above, made of plastic materials and intended for use with power-driven syringe pumps. This document does not apply to syringes with auto-disable syringe features...

DS/ISO 7886-2 - Sterile hypodermic syringes for single use – Part 2: Syringes for use with power-driven syringe pumps
May 18, 2020 - DS

This document specifies requirements for sterile single-use hypodermic syringes of nominal capacity 1 ml and above, made of plastic materials and intended for use with power-driven syringe pumps. This document does not apply to syringes with auto-disable syringe features...

DS/EN ISO 7886-2 - Sterile hypodermic syringes for single use – Part 2: Syringes for use with power-driven syringe pumps (ISO 7886-2:2020)
May 18, 2020 - DS

This document specifies requirements for sterile single-use hypodermic syringes of nominal capacity 1 ml and above, made of plastic materials and intended for use with power-driven syringe pumps. This document does not apply to syringes with auto-disable syringe features...

DS/EN ISO 80369-3 - Small-bore connectors for liquids and gases in healthcare applications – Part 3: Connectors for enteral applications (ISO 80369-3:2016)
August 25, 2016 - DS

ISO 80369-3:2016 specifies the dimensions and requirements for the design and functional performance of small-bore connectors intended to be used for connections on enteral medical devices and accessories. NOTE 1 - Enteral medical devices include enteral feeding sets, enteral drainage...

CEI UNI EN ISO 80369-3 - Small-bore connectors for liquids and gases in healthcare applications Part 3: Connectors for enteral applications
January 1, 2017 - CEI

This part of ISO 80369 specifies the dimensions and requirements for the design and functional performance of SMALL-BORE CONNECTORS intended to be used for CONNECTIONS on ENTERAL MEDICAL DEVICES and ACCESSORIES. NOTE 1 ENTERAL MEDICAL DEVICES include ENTERAL feeding sets, ENTERAL...

DSF/ISO/DIS 11608-1 - Needle-based injection systems for medical use – Requirements and test methods – Part 1: Needle-based injection systems
DS

This document specifies requirements and test methods for Needle-Based Injection Systems (NISs) for single-patient use intended to deliver discrete volumes (bolus) of medicinal product, through needles or soft cannulas for intradermal, subcutaneous and/or intramuscular delivery, incorporating...

ISO 11040-7 - Prefilled syringes - Part 7: Packaging systems for sterilized subassembled syringes ready for filling
April 1, 2015 - ISO

This part of ISO 11040 specifies the packaging system that is used to deliver sterilized subassembled syringes ready for filling in tubs and nests. Downstream processes (processes after filling such as in house/outside transport, reprocessing) can result in specific requirements on the...

ISO 18250-7 - Medical devices - Connectors for reservoir delivery systems for healthcare applications - Part 7: Connectors for intravascular infusion
December 1, 2018 - ISO

This document specifies the interface dimensions and requirements for the design and functional performance of connectors intended to be used to connect intravascular infusion sets to intravascular infusion reservoirs. This document does not specify the dimensions and requirements for the...

DS/EN ISO 23907 - Sharps injury protection – Requirements and test methods – Sharps containers
October 11, 2012 - DS

ISO 23907:2012 specifies requirements for single-use sharps containers intended to hold potentially hazardous sharps medical waste with or without sharps protection features, e.g. scalpel blades, trocars, hypodermic needles and syringes. It is applicable to sharps containers that are...

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