Guidance note for the registration of persons responsible for placing devices on the market in accordance with Directive 93/42/EEC and S.I. No. 252 of 1994
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 note2