|
|
|
|
Product | ISO 18113-1:2022 | ||
---|---|---|---|
Price | Price USD 215.00 | ||
Rating | Rating | ||
Buy | Buy Add to Cart | ||
Description |
Description
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). |
||
Standard Number | Standard Number ISO 18113-1:2022 | ||
Title | Title ISO 18113-1:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements | ||
Status | Status Published | ||
Publication Date | Publication Date 06 Oct 2022 | ||
Cross References | Cross References | ||
Descriptors | Descriptors | ||
ICS | ICS 11.100.10 | ||
Committee | Committee ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems | ||
ISBN | ISBN | ||
Publisher | Publisher PECB Store | ||
Format | Format PDF | ||
Delivery | Delivery NO | ||
Pages | Pages 53 | ||
File Size | File Size KB |