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DIN EN ISO 19001:2013-07

Current
Current

The latest, up-to-date edition.

IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR STAINING IN BIOLOGY (ISO 19001:2013)
Available format(s)

Hardcopy , PDF

Language(s)

German, English

Published date

01-07-2013

National foreword
National Annex NA (informative) - Bibliography
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements for information supplied by the
  manufacturer
Annex A (informative) - Examples of information
        supplied by the manufacturer with reagents
        commonly used in biological staining
        procedures
Bibliography

This standard is included in DIN HDBK 378.

Committee
TC 212
DevelopmentNote
Supersedes DIN EN 12376. (07/2013)
DocumentType
Standard
Pages
20
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Current
Supersedes

Standards Relationship
EN ISO 19001:2013 Identical
ISO 19001:2013 Identical
PREN ISO 19001 : DRAFT 2010 Identical

ISO 80000-9:2009 Quantities and units Part 9: Physical chemistry and molecular physics
ISO 18113-1:2009 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
DIN EN ISO 18113-2:2013-01 IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 2: IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE (ISO 18113-2:2009)
ISO 80000-1:2009 Quantities and units — Part 1: General
ISO 18113-2:2009 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
DIN EN ISO 18113-1:2013-01 IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS (ISO 18113-1:2009)

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