EN ISO 8536-10:2015
Current
The latest, up-to-date edition.
Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment (ISO 8536-10:2015)
17-06-2015
Foreword
1 Scope
2 Normative references
3 Materials
4 Physical requirements
5 Chemical requirements
6 Biological requirements
7 Packaging
8 Labelling
9 Disposal
Annex A (normative) - Physical tests
Annex B (normative) - Chemical tests
Annex C (normative) - Biological tests
Annex ZA (informative) - Relationship between this
European Standard and the Essential Requirements
of EU Directive 93/42/EEC on Medical devices
Bibliography
ISO 8536-10:2015 applies to sterilized accessories for single use in fluid lines and pressure infusion equipment as specified in ISO 8536-8.ISO 8536-10:2015 includes the following:a) two-way stopcocks, three-way stopcocks, four-way stopcocks, and stopcocks manifold;b) units with injection site or check valve;c) stoppers or adapters.
| Committee |
CEN/TC 205
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Standards | Relationship |
| ISO 8536-10:2015 | Identical |
| NBN EN ISO 8536-10 : 2015 | Identical |
| NF EN ISO 8536-10 : 2015 | Identical |
| NEN EN ISO 8536-10 : 2015 | Identical |
| NS EN ISO 8536-10 : 2004 | Identical |
| I.S. EN ISO 8536-10:2015 | Identical |
| PN EN ISO 8536-10 : 2015 | Identical |
| BS EN ISO 8536-10:2015 | Identical |
| DIN EN ISO 8536-10:2015-11 | Identical |
| UNE-EN ISO 8536-10:2015 | Identical |
| BS EN ISO 8536-9:2015 | Infusion equipment for medical use Fluid lines for single use with pressure infusion equipment |
| I.S. EN ISO 8536-9:2015 | INFUSION EQUIPMENT FOR MEDICAL USE - PART 9: FLUID LINES FOR SINGLE USE WITH PRESSURE INFUSION EQUIPMENT (ISO 8536-9:2015) |
| EN ISO 8536-9:2015 | Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment (ISO 8536-9:2015) |
| ISO 8536-9:2015 | Infusion equipment for medical use — Part 9: Fluid lines for single use with pressure infusion equipment |
| UNE-EN ISO 8536-9:2015 | Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment (ISO 8536-9:2015) |
| ISO 11137-1:2006 | Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices |
| ISO 8536-12:2007 | Infusion equipment for medical use — Part 12: Check valves |
| ISO 10993-4:2017 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood |
| EN 15986:2011 | Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates |
| ISO 8536-8:2015 | Infusion equipment for medical use — Part 8: Infusion sets for single use with pressure infusion apparatus |
| EN ISO 8536-8:2015 | Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus (ISO 8536-8:2015) |
| EN ISO 10993-4:2017 | Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) |
| 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 |
| ISO 11137-2:2013 | Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose |
| ISO 8536-4:2010 | Infusion equipment for medical use — Part 4: Infusion sets for single use, gravity feed |
| 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 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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