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

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Manufacturer's Devices - Albomed GMBH

Address:

Hildebrandstrasse 11

Schwarzenbruck

D-90592

Germany

Authorised Representative/ UK Responsible Person
Name: Vision Pharmaceuticals Ltd (Spectrum)
Address:

Fernbank House Tytherington Business Park

Springwood Way

Macclesfield

Cheshire SK10 2XA

England United Kingdom

Code/Term Type

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

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
Aqueous/vitreous humour replacement medium kit	Aqueous/vitreous humour replacement medium kit	Class IIa
Synovial fluid supplementation medium	Synovial fluid supplementation medium	Class III