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Product | ISO 18113-5:2022 | ||
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Price | Price USD 69.00 | ||
Rating | Rating | ||
Buy | Buy Add to Cart | ||
Description |
Description
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for self-testing. This document is also applicable to apparatus and equipment intended to be used with IVD instruments for self-testing. This document can also be applicable to accessories. This document does not apply to: a) instructions for instrument servicing or repair; b) IVD reagents, including calibrators and control materials for use in control of the reagent; c) IVD instruments for professional use. |
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Standard Number | Standard Number ISO 18113-5:2022 | ||
Title | Title ISO 18113-5:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing | ||
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 10 | ||
File Size | File Size KB |