Back

ISO/TS 16775:2014

Packaging for terminally sterilized medical devices -- Guidance on the application of ISO 11607-1 and ISO 11607-2

General information
Withdrawn from 05.11.2021
Directives or regulations
None

Standard history

Status
Date
Type
Name
05.11.2021
Main
09.05.2014
Main
ISO/TS 16775:2014 provides guidance for the application of the requirements contained in ISO 11607-1 and ISO 11607-2. It does not add to, or otherwise change, the requirements of ISO 11607-1 and/or ISO 11607-2. It is an informative document, not normative, and does not include requirements to be used as basis of regulatory inspection or certification assessment activities.
The guidance can be used to better understand the requirements of ISO 11607-1 and/or ISO 11607-2 and illustrates some of the variety of methods and approaches available for meeting the requirements of those International Standards. It is not required to be used to demonstrate compliance with them.
Guidelines are given for evaluation, selection and use of packaging materials, preformed sterile barrier systems, sterile barrier systems and packaging systems. Guidance on validation requirements for forming, sealing and assembly processes is also given.
ISO/TS 16775:2014 provides information for health care facilities and for the medical devices industry. It does not provide guidance for applications of packaging materials and systems after their opening. In the use of packaging for other purposes such as a "sterile field" or transport of contaminated items, other regulatory standards will apply.
*
*
*
PDF
79.98 € incl tax
Paper
79.98 € incl tax
Standard monitoring

Customers who bought this item also bought

Main

ISO/TR 16197:2014

Nanotechnologies -- Compilation and description of toxicological screening methods for manufactured nanomaterials
Newest version Valid from 12.05.2014
Main

EVS-EN ISO 7864:1999

Sterile hypodermic needles for single use
Withdrawn from 04.10.2016
Main

ISO/TS 10993-20:2006

Biological evaluation of medical devices -- Part 20: Principles and methods for immunotoxicology testing of medical devices
Newest version Valid from 03.08.2006
Main

ISO 10993-2:2006

Biological evaluation of medical devices -- Part 2: Animal welfare requirements
Withdrawn from 03.11.2022