BSI - BS ISO 17218
Sterile acupuncture needles for single use
active, Most Current
Buy Now
| Organization: | BSI |
| Publication Date: | 31 May 2014 |
| Status: | active |
| Page Count: | 36 |
| ICS Code (Syringes, needles and catheters): | 11.040.25 |
Document History
BS ISO 17218
May 31, 2014
Sterile acupuncture needles for single use
A description is not available for this item.
References
This document references:
EEC/2007/47 - DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market
Published by EEC
on
September 5, 2007
A description is not available for this item.
This document references:
ISO 780 - Packaging - Distribution packaging - Graphical symbols for handling and storage of packages
Published by ISO
on
December 1, 2015
This International Standard specifies a set of graphical symbols conventionally used for marking of distribution packages in their physical distribution chain to convey handling instructions. The...
This document references:
EN 10088-1 - Stainless steels - Part 1: List of stainless steels
Published by CEN
on
October 1, 2014
This European Standard lists the chemical composition of stainless steels, which are subdivided in accordance with their main properties into corrosion resisting steels, heat resisting steels and...
This document references:
ISO 11138-2 - Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes
Published by ISO
on
March 1, 2017
This document specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilizers and...
This document references:
ISO 11607-2 - Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
Published by ISO
on
February 1, 2019
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
This document references:
EN 10088-1 - Stainless steels - Part 1: List of stainless steels
Published by CEN
on
October 1, 2014
This European Standard lists the chemical composition of stainless steels, which are subdivided in accordance with their main properties into corrosion resisting steels, heat resisting steels and...
This document references:
ISO 780 - Packaging - Distribution packaging - Graphical symbols for handling and storage of packages
Published by ISO
on
December 1, 2015
This International Standard specifies a set of graphical symbols conventionally used for marking of distribution packages in their physical distribution chain to convey handling instructions. The...
This document references:
ISO 11138-2 - Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes
Published by ISO
on
March 1, 2017
This document specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilizers and...
This document references:
ISO 11607-2 - Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
Published by ISO
on
February 1, 2019
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
This document references:
EEC/2007/47 - DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market
Published by EEC
on
September 5, 2007
A description is not available for this item.