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DIN EN 980:2003-08

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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
Available format(s)

Hardcopy , PDF

Superseded date

01-10-2012

Language(s)

English

Published date

01-01-2003

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Superseded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
SN EN 980 : 2008 Identical
NF EN 980 : 2008 Identical
UNI EN 980 : 2004 Identical
UNE-EN 980:2008 Identical
EN 980:2008 Identical
I.S. EN 980:2008 Identical
NS EN 980 : 3ED 2008 Identical

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

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