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 - Bio-Technology General Ltd.

Address:

Be'er Tuvia Industrial Zone P.O. Box 571

Kiryat Malachi 8310402

8310402

Israel

Authorised Representative/ UK Responsible Person
Name: Ferring Pharmaceuticals Ltd
Address:

Drayton Hall Church Road

West Drayton

West Drayton

UB7 7PS

England United Kingdom

Code/Term Type

Synovial fluid supplementation medium Synovial fluid supplementation medium Class III

Vitreous/aqueous humour replacement medium intraoperative Vitreous/aqueous humour replacement medium intraoperative Class IIb

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
Synovial fluid supplementation medium	Synovial fluid supplementation medium	Class III
Vitreous/aqueous humour replacement medium intraoperative	Vitreous/aqueous humour replacement medium intraoperative	Class IIb