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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:
01/15/2010

Status:
[ Revised ]

Description:

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

Publisher:
Dansk Standard

Document status:
Active
Format:
Electronic (PDF)
Delivery time:
10 minutes
Delivery time (for Russian version):
200 business days
SKU:
Choose Document Language:
$33
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This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This part of ISO 18113 does not address language requirements, since that is the domain of national laws and regulations. This part of ISO 18113 does not apply to a) IVD devices for performance evaluation (e.g., for investigational use only), b) instrument marking, c) material safety data sheets.


Edition : 10
File Size : 1 file , 1.7 MB
Number of Pages : 66
Product Code(s) : DS-061, DS-061
Published : 01/15/2010

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
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)
$20.7
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
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

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