Log inSign up
LANGUAGE en
Menu
STOREE-ReadingHelp centerContactsDelivery chargesABOUT US News
SEARCH
0
Total price
0 EUR
PRICES include / exclude VAT
Homepage>ISO Standards>ISO 18113-4:2022-In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)-Part 4: In vitro diagnostic reagents for self-testing
Sponsored link
download between 0-24 hoursReleased: 2022
ISO 18113-4:2022-In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)-Part 4: In vitro diagnostic reagents for self-testing

ISO 18113-4:2022

ISO 18113-4:2022-In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)-Part 4: In vitro diagnostic reagents for self-testing

Format
Availability
Price and currency
English PDF
Immediate download
70.00 EUR
English Hardcopy
In stock
70.00 EUR
French PDF
Immediate download
70.00 EUR
French Hardcopy
In stock
70.00 EUR
Standard´s number:ISO 18113-4:2022
Pages:11
Edition:2
Released:2022
DESCRIPTION

ISO 18113-4:2022


This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents, calibrators, and controls intended for self-testing. 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 professional use.
Print