DIN EN ISO 18113-1 PDF

Name:
DIN EN ISO 18113-1 PDF

Published Date:
10/01/2024

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:
DIN-adopted European-adopted ISO Standard

Document status:

Active

Format:

Electronic (PDF)

Delivery time:

10 minutes

Delivery time (for Russian version):

200 business days

SKU:

File Size :	1 file , 2.7 MB
Note :	This product is unavailable in Ukraine, Russia, Belarus
Number of Pages :	68
Product Code(s) :	3370946, 3569220, 3370946, 3569220, 3370946, 3569220
Published :	10/01/2024

History

DIN EN ISO 18113-1

Published Date: 10/01/2024

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

$69.324

DIN EN ISO 18113-1 - DRAFT

Published Date: 09/01/2021

Draft Document - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/DIS 18113-1:2021); German and English version prEN ISO 18113-1:2021

172.66 166.77 you save 5.89

DIN EN ISO 18113-1

Published Date: 01/01/2013

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2011

$55.59

DIN EN ISO 18113-1

Published Date: 05/01/2010

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

$57.552

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