Public Access Database for Medical Device Registration

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 - IDL biotech

Address:

IDL Biotech PO BOX 11151

Karlsbodavagen 39

Bromma

SE 161 11

Sweden

Authorised Representative/ UK Responsible Person
Name: Rock Medical
Address:

Melton Lodge New Road

Hurley

SL6 5LN

England United Kingdom

Code/Term Type

Bladder tumour associated antigen IVD kit rapid ICT clinical Bladder tumour associated antigen IVD kit rapid ICT clinical IVD General

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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