BS ISO 25841:2017

Superseded

View Superseded by

Female condoms. Requirements and test methods

Available format(s)

Hardcopy , PDF

Superseded date

04-11-2020

Language(s)

English

Published date

09-18-2017

Publisher

British Standards Institution

Committee	CH/157
DevelopmentNote	Supersedes 15/30303073 DC. (10/2017)
DocumentType	Standard
Pages	66
PublisherName	British Standards Institution
Status	Superseded
SupersededBy	BS ISO 25841:2017+A1:2020
Supersedes	15/30303073 DC : 0 BS ISO 25841:2014

Standards	Relationship
ISO 25841:2017	Identical

ISO 10993-3:2014	Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
ISO 11346:2014	Rubber, vulcanized or thermoplastic — Estimation of life-time and maximum temperature of use
ISO 11737-1:2006	Sterilization of medical devices Microbiological methods Part 1: Determination of a population of microorganisms on products
ISO 13485:2016	Medical devices Quality management systems Requirements for regulatory purposes
ISO 188:2011	Rubber, vulcanized or thermoplastic — Accelerated ageing and heat resistance tests
ISO 2230:2002	Rubber products — Guidelines for storage
EN 1041:2008+A1:2013	Information supplied by the manufacturer of medical devices
ISO 10993-10:2010	Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
ISO 9004:2009	Managing for the sustained success of an organization A quality management approach
ISO 10993-11:2017	Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
ISO 10993-1:2009	Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ISO 4074:2015	Natural rubber latex male condoms Requirements and test methods
ISO 9001:2015	Quality management systems — Requirements
ISO 9000:2015	Quality management systems — Fundamentals and vocabulary
ISO 14155:2011	Clinical investigation of medical devices for human subjects Good clinical practice
ISO/IEC 17007:2009	Conformity assessment — Guidance for drafting normative documents suitable for use for conformity assessment
ISO/TR 8550-1:2007	Guidance on the selection and usage of acceptance sampling systems for inspection of discrete items in lots Part 1: Acceptance sampling
ISO/TR 8550-2:2007	Guidance on the selection and usage of acceptance sampling systems for inspection of discrete items in lots Part 2: Sampling by attributes
ISO 14971:2007	Medical devices Application of risk management to medical devices
ISO 29943-2:2017	Condoms — Guidance on clinical studies — Part 2: Female condoms, clinical function studies based on self-reports