DIN EN 980:2003-08
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES
Hardcopy , PDF
English
01-01-2003
01-10-2012
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Symbols already in use
6 New symbols
Annex A (informative) - Examples of uses of symbols given in
this standard
Annex B (informative) - Use of the general prohibition symbol
and the negation symbol
Annex ZA (informative) - Clauses of this European Standard
addressing essential requirements or other provisions of
the Council Directive 93/42/EEC concerning medical devices
Annex ZB (informative) - Clauses of this European Standard
addressing essential requirements or other provisions of
the Council Directive 90/385/EEC relating to active
implantable medical devices
Annex ZC (informative) - Clauses of this European Standard
addressing essential requirements or other provisions of
the European Parliament and the Council Directive 98/79/EC
on in vitro diagnostic medical devices
Bibliography
Defines graphical symbols to be used on information supplied with medical devices by the manufacturer.
| DocumentType |
Standard
|
| Pages |
25
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Superseded
|
| Standards | Relationship |
| NBN EN 980 : 2008 | Identical |
| NEN EN 980 : 2008 | Identical |
| BS EN 980:2008 | Identical |
| NF EN 980 : 2008 | Identical |
| EN 980:2008 | Identical |
| I.S. EN 980:2008 | Identical |
| NS EN 980 : 3ED 2008 | Identical |
| I.S. EN 980:2003 | Equivalent |
| EN 60417-1:2002 | GRAPHICAL SYMBOLS FOR USE ON EQUIPMENT - PART 1: OVERVIEW AND APPLICATION |
| EN 376 : 2002 | INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING |
| EN 60417-2:1999 | Graphical symbols for use on equipment - Part 2: Symbol originals |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| EN 375 : 2001 | INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE |
| EN 61010-1:2010 | Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements |
| ISO 7000:2014 | Graphical symbols for use on equipment — Registered symbols |
| EN 80416-1:2009 | Basic principles for graphical symbols for use on equipment - Part 1: Creation of graphical symbols for registration |
| EN 28601 : 1992 | DATA ELEMENTS AND INTERCHANGE FORMATS - INFORMATION INTERCHANGE - REPRESENTATION OF DATES AND TIMES |
| ISO 15223:2000 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied |
Access your standards online with a subscription
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.
Important note : Users cannot be edited or removed once added to your Multi user PDF.