Guidance note for the registration of persons responsible for placing in-vitro diagnostic medical devices on the market in accordance with Directive 98/79/EC and S.I. No. 304 of 2001.
Authors
Irish Medicines Board (IMB)Issue Date
2004-10-21Keywords
MEDICAL DEVICESREGULATION
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Irish Medicines Board (IMB)Item Type
OtherLanguage
enSeries/Report no.
Guidance note3