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 - Bürki inno med AG

Address:

Industriestrasse 67

Widnau

St. Gallen 9443

Switzerland

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Ophthalmic surgical irrigation/infusion/aspiration handle single-use Ophthalmic surgical irrigation/infusion/aspiration handle single-use Class IIa

Ophthalmic irrigation/infusion/aspiration cannula non-illuminating reusable Ophthalmic irrigation/infusion/aspiration cannula non-illuminating reusable Class IIa

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
Ophthalmic surgical irrigation/infusion/aspiration handle single-use	Ophthalmic surgical irrigation/infusion/aspiration handle single-use	Class IIa
Ophthalmic irrigation/infusion/aspiration cannula non-illuminating reusable	Ophthalmic irrigation/infusion/aspiration cannula non-illuminating reusable	Class IIa