Fees in Respect of Dealer’s Licences Regulations
Version of section 41 from 2011-04-01 to 2020-03-31:
Marginal note:Fee — amendment to medical device licence
41 The fee that is payable by a manufacturer for the examination of an application for a licence amendment submitted in accordance with paragraph 34(a) or (b) of the Medical Devices Regulations is
(a) in the case of a Class III medical device, the amount obtained by adding, for each category set out in column 1 of Schedule 6, the fee set out in column 2; or
(b) in the case of a Class IV medical device, the amount obtained by adding, for each category set out in column 1 of Schedule 7, the fee set out in column 2.
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