UNE-EN ISO 3826-1:2013
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013)
Available format(s)
Hardcopy , PDF
Language(s)
English, Spanish, Castilian
Published date
12-11-2013
Publisher
Superseded date
07-15-2020
US$109.44
Excluding Tax where applicable
| Committee |
CTN 111
|
| DocumentType |
Standard
|
| Pages |
33
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Superseded
|
| Standards | Relationship |
| NS EN ISO 3826-1 : 2013 | Identical |
| ISO 3826-1:2013 | Identical |
| DIN EN ISO 3826-1:2013-09 | Identical |
| ONORM EN ISO 3826-1 : 2013 | Identical |
| I.S. EN ISO 3826-1:2013 | Identical |
| BS EN ISO 3826-1:2013 | Identical |
| NBN EN ISO 3826-1 : 2013 | Identical |
| EN ISO 3826-1:2013 | Identical |
| NEN EN ISO 3826-1 : 2013 | Identical |
| NF EN ISO 3826-1 : 2013 | Identical |
| ISO 3826-2:2008 | Plastics collapsible containers for human blood and blood components — Part 2: Graphical symbols for use on labels and instruction leaflets |
| 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 9626:2016 | Stainless steel needle tubing for the manufacture of medical devices — Requirements and test methods |
| ISO 3826-3:2006 | Plastics collapsible containers for human blood and blood components — Part 3: Blood bag systems with integrated features |
| ISO 10993-10:2010 | Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization |
| ISO 10993-11:2017 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity |
| ISO 10993-12:2012 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials |
| ISO 10993-1:2009 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process |
| ISO 1135-4:2015 | Transfusion equipment for medical use — Part 4: Transfusion sets for single use, gravity feed |
| ISO 3696:1987 | Water for analytical laboratory use — Specification and test methods |
| ISO 15223-1:2016 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Part 1: General requirements |
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