Abstract
PreviewThis 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).
.
-
Status: PublishedPublication date: 2022-10
-
Edition: 2Number of pages: 53
-
- ICS :
- 11.100.10 In vitro diagnostic test systems
Buy this standard
en
| Format | Language | |
|---|---|---|
| std 1 187 | PDF + ePub | |
| std 2 187 | Paper |
- CHF187
Life cycle
-
Previously
WithdrawnISO 18113-1:2009
-
Now
Got a question?
Check out our FAQs
Customer care
+41 22 749 08 88
Opening hours:
Monday to Friday - 09:00-12:00, 14:00-17:00 (UTC+1)