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DIN EN ISO 8536-4:2013-07

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010 + AMD 1:2013)

Available format(s)

Hardcopy , PDF

Superseded date

26-01-2021

Language(s)

German, English

Published date

01-07-2013

$196.06
Including GST where applicable

This standard is included in DIN Handbook 227/1 and 463.

Committee
TC 76
DevelopmentNote
Supersedes DIN 58362-1 (03/2005) DRAFT 2018 issued in April 2018. (05/2018)
DocumentType
Standard
Pages
26
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded
SupersededBy
Supersedes

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DIN ISO 8536-5:2006-04 INFUSION EQUIPMENT FOR MEDICAL USE - PART 5: BURETTE INFUSION SETS FOR SINGLE USE, GRAVITY FED
DIN EN ISO 8536-5:2013-10 INFUSION EQUIPMENT FOR MEDICAL USE - PART 5: BURETTE INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-5:2004)
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ISO 7864:2016 Sterile hypodermic needles for single use — Requirements and test methods
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ISO 291:2008 Plastics Standard atmospheres for conditioning and testing
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ISO 3696:1987 Water for analytical laboratory use — Specification and test methods
ISO/TS 11135-2:2008 Sterilization of health care products Ethylene oxide Part 2: Guidance on the application of ISO 11135-1
ISO 7000:2014 Graphical symbols for use on equipment Registered symbols
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
DIN ISO 3696:1991-06 WATER FOR ANALYTICAL LABORATORY USE - SPECIFICATION AND TEST METHODS
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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