BS ISO 28620:2010
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Medical devices. Non-electrically driven portable infusion devices
Hardcopy , PDF
20-01-2020
English
28-02-2010
Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Operating requirements
6 Test methods
7 Information to be listed on packaging and/or product
8 Accompanying documents
Bibliography
Describes essential requirements and related test methods for non-electrically driven portable infusion devices.
Committee |
CH/212
|
DevelopmentNote |
Supersedes 08/30170025 DC. (09/2010)
|
DocumentType |
Standard
|
Pages |
20
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
ISO 28620:2010 | Identical |
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 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 |
EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
ISO 10555-1:2013 | Intravascular catheters — Sterile and single-use catheters — Part 1: General requirements |
IEC 60601-2-24:2012 | Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers |
ISO 554:1976 | Standard atmospheres for conditioning and/or testing — Specifications |
ISO 11607-1:2006 | Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems |
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 |
EN 13868:2002 | Catheters - Test methods for kinking of single lumen catheters and medical tubing |
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 |
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