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DANSK DS/EN ISO 18113-1 PDF

DANSK DS/EN ISO 18113-1 PDF

Name:
DANSK DS/EN ISO 18113-1 PDF

Published Date:
06/18/2024

Status:
[ Active ]

Description:

In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Publisher:
Dansk Standard

Document status:
Active
Format:
Electronic (PDF)
Delivery time:
10 minutes
Delivery time (for Czech version):
200 business days
SKU:
dansk-ds-en-iso-18113-1_2914525
Choose Document Language:
33.00 €
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SAME AS ISO 18113-1

This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This document does not address language requirements since that is the domain of national laws and regulations. This document does not apply to: a) IVD medical devices for performance evaluation (e.g. for investigational use only); b) shipping documents; c) material safety data sheets / Safety Data Sheets; d) marketing information (consistent with applicable legal requirements). .


Edition : 24#
File Size : 1 file , 2 MB
Number of Pages : 68
Product Code(s) : DS-061, DS-061
Published : 06/18/2024

History

DANSK DS/EN ISO 18113-1
DANSK DS/EN ISO 18113-1
Published Date: 06/18/2024
In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)
33.00 €
DANSK DSF/PREN ISO 18113-1
DANSK DSF/PREN ISO 18113-1
Published Date:
In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 1: Terms, definitions, and general requirements (ISO/DIS 18113-1:2021)
20.70 €
DANSK DS/EN ISO 18113-1
DANSK DS/EN ISO 18113-1
Published Date: 12/09/2011
In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 1: Terms, definitions and general requirements
33.00 €
DANSK DS/EN ISO 18113-1
DANSK DS/EN ISO 18113-1
Published Date: 01/15/2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
33.00 €

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