ISO 11040-6:2012

Withdrawn

View Superseded by

Prefilled syringes Part 6: Plastic barrels for injectables

Available format(s)

Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users

Withdrawn date

01-12-2019

Language(s)

English, French

Published date

03-29-2012

Publisher

International Organization for Standardization

DevelopmentNote	DRAFT ISO/DIS 11040-6 is also available for this standard. (08/2017)
DocumentType	Standard
Pages	10
PublisherName	International Organization for Standardization
Status	Withdrawn
SupersededBy	ISO 11040-6:2019

Standards	Relationship
NEN ISO 11040-6 : 2012	Identical
BS ISO 11040-6:2012	Identical
NF ISO 11040-6 : 2012	Identical

ISO 11040-8:2016	Prefilled syringes — Part 8: Requirements and test methods for finished prefilled syringes
15/30304642 DC : 0	BS ISO 11040-8 - PREFILLED SYRINGES - PART 8: REQUIREMENTS AND TEST METHODS FOR FINISHED PRIFILLED SYRINGES

ISO 11040-4:2015	Prefilled syringes Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling
ISO 11040-5:2012	Prefilled syringes — Part 5: Plunger stoppers for injectables
ISO 14937:2009	Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
ISO 11040-7:2015	Prefilled syringes Part 7: Packaging systems for sterilized subassembled syringes ready for filling
ASTM D 7210 : 2013 : REDLINE	Standard Practice for Extraction of Additives in Polyolefin Plastics
ISO 3826-1:2013	Plastics collapsible containers for human blood and blood components Part 1: Conventional containers
ISO 11135-1:2007	Sterilization of health care products Ethylene oxide Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
ISO 7886-1:2017	Sterile hypodermic syringes for single use — Part 1: Syringes for manual use
ISO 15378:2017	Primary packaging materials for medicinal products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
ISO 13926-2:2011	Pen systems Part 2: Plunger stoppers for pen-injectors for medical use
ISO 10993-1:2009	Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ISO 80369-7:2016	Small-bore connectors for liquids and gases in healthcare applications Part 7: Connectors for intravascular or hypodermic applications
ISO 594-2:1998	Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 2: Lock fittings
ISO 15223-1:2016	Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements
ISO 594-1:1986	Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements
ISO 15747:2010	Plastic containers for intravenous injections
ISO 17665-1:2006	Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices