In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009, IDT)
This Malaysian Standard specifies requirements for information supplied by the manufacturer of IVD reagents for professional use.
This standard also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.
Published
• (none) / (none) / (none)
PDF
17/01/2021
19
NSC 18 - Medical Devices and Facilities for Healthcare
