CEI UNI EN ISO 15223-1:2022-07
Current
Current
The latest, up-to-date edition.
Medical devices - Symbols to be used with information to be supplied by the manufacturer Part 1: General requirements
Available format(s)
PDF
Language(s)
English
Published date
01-09-2022
Publisher
US$190.08
Excluding Tax where applicable
This document specifies symbols used to express information supplied for a medical device.
| Committee |
CT 62
|
| DocumentType |
Standard
|
| Pages |
68
|
| PublisherName |
Comitato Elettrotecnico Italiano
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| EN ISO 15223-1:2021 | Identical |
| ISO 15223-1:2021 | Identical |
| IEC TR 60878:2003 | Graphical symbols for electrical equipment in medical practice |
| ISO 14971:2019 | Medical devices — Application of risk management to medical devices |
| ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements |
| EN 556-1:2001 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices |
| ISO 13485:2016 | Medical devices — Quality management systems — Requirements for regulatory purposes |
| ISO 18113-4:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing |
| ISO 20417:2021 | Medical devices — Information to be supplied by the manufacturer |
| ISO 7010:2003 | Graphical symbols — Safety colours and safety signs — Safety signs used in workplaces and public areas |
| IEC 62570:2014 | Standard practice for marking medical devices and other items for safety in the magnetic resonance environment |
| EN 1041:2008 | Information supplied by the manufacturer of medical devices |
| ISO 7001:2007 | Graphical symbols — Public information symbols |
| ISO 11607-1:2019 | Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems |
| ISO 7000:2019 | Graphical symbols for use on equipment — Registered symbols |
| ISO 18113-2:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use |
| ISO 3864-1:2011 | Graphical symbols — Safety colours and safety signs — Part 1: Design principles for safety signs and safety markings |
| ISO 11607-2:2019 | Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes |
| ISO 18113-5:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing |
| ISO 18113-3:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use |
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