Registration number (WIID)Project No.TitleStatus
5099EN 376:2002Information supplied by the manufacturer with in vitro diagnostic reagents for self-testingAtcelts
24452EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006)Atcelts
5096EN 1658:1996Requirements for marking of in vitro diagnostic instrumentsAtcelts
62543LVS EN ISO 22870:2017Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016)Atcelts
5094EN 591:1994In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional useAtcelts
5075EN 829:1996In vitro diagnostic systems - Transport packages for medical and biological specimens - Requirements, testsAtcelts
23415LVS EN ISO 20776-1:2007Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesAtcelts
25659LVS EN ISO 15189:2007 AMedical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
5108EN ISO 15197:2003In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)Atcelts
24023EN ISO 15197:2003/AC:2005In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)Atcelts
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