NEN EN 375 : 2001
Withdrawn
Withdrawn
INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN-VITRO-DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE
Published date
01-12-2013
Publisher
Withdrawn date
07-05-2012
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Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements for labels
4.1 Outer container
4.2 Immediate container
5 Requirements for instructions for use
Annex ZA (informative) Relationship of this document
with EC Directives
Bibliography
Defines the requirements for the information supplied by the manufacturer of in vitro diagnostic reagents that includes reagent products, calibrators, control materials and kits for professional use, hereafter called IVD reagents. Also applicable to accessories.
| DocumentType |
Standard
|
| PublisherName |
Netherlands Standards
|
| Status |
Withdrawn
|
| Standards | Relationship |
| I.S. EN 375:2001 | Identical |
| UNE-EN 375:2001 | Identical |
| BS EN 375:2001 | Identical |
| EN 375 : 2001 | Identical |
| DIN EN 375:2001-06 | Identical |
Summarise
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