Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity
Manufacturer's By Name
By Device
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Manufacturer's Devices - PARMR LTD
Address:
10 Clover Way Syston
Leicester
Leicestershire LE7 2BR
England United Kingdom
Authorised Representative/ UK Responsible Person
Name: Not Available
Address:
Code/Term
Type
Hip/knee/ankle/foot orthosis
Hip/knee/ankle/foot orthosis
Class I