ISO/TS 16775:2014

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

Publication date:   May 9, 2014

95.99 Withdrawal of Standard   Nov 5, 2021

General information

95.99 Withdrawal of Standard   Nov 5, 2021

ISO

ISO/TC 198 Sterilization of health care products

Technical Specification

11.080.30   Sterilized packaging

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Scope

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.

Life cycle

NOW

WITHDRAWN
ISO/TS 16775:2014
95.99 Withdrawal of Standard
Nov 5, 2021

REVISED BY

PUBLISHED
ISO/TS 16775:2021