Public Access Database for Medical Device Registration

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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 - VSY Biotechnology GmbH

Address:

Esslinger Str 7

Leinfelden-Echterdingen

D-70771

Germany

Authorised Representative/ UK Responsible Person
Name: Daybreak Medical Ltd
Address:

Unit 4 St Lawrence Business Centre Victoria Road

Feltham

TW13 7LT

England United Kingdom

Code/Term Type

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

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