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 - Bohus BioTech AB

Address:

Trädgårdsgatan 4

Strömstad

45231

Sweden

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Dermal tissue reconstructive material microbe-derived Dermal tissue reconstructive material microbe-derived Class III

Aqueous/vitreous humour replacement medium kit Aqueous/vitreous humour replacement medium kit Class III

Eye lubricant Eye lubricant Class IIb

Synovial fluid supplementation medium Synovial fluid supplementation medium Class III

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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Code/Term		Type
Dermal tissue reconstructive material microbe-derived	Dermal tissue reconstructive material microbe-derived	Class III
Aqueous/vitreous humour replacement medium kit	Aqueous/vitreous humour replacement medium kit	Class III
Eye lubricant	Eye lubricant	Class IIb
Synovial fluid supplementation medium	Synovial fluid supplementation medium	Class III