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Homepage>CSN Standards>85 HEALTH SERVICE>8570 Diagnostic systems in vitro>CSN EN ISO 18113-2 ed. 2 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
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Released: 01.11.2024
CSN EN ISO 18113-2 ed. 2 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use

CSN EN ISO 18113-2 ed. 2

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use

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Number of Standard:CSN EN ISO 18113-2 ed. 2
Category:857027
Pages:28
Released:01.11.2024
Catalog number:519960
DESCRIPTION

CSN EN ISO 18113-2 ed. 2

CSN EN ISO 18113-2 ed. 2 This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents, calibrators and controls intended for professional use. This document can also be applicable to accessories. This document is applicable to the labels for outer and immediate containers and to the instructions for use. This document does not apply to: a) IVD instruments or equipment; b) IVD reagents for self-testing.
Original English text of CSN EN Standard.
The price of the Standard included all amendments and correcturs.
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