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 - Geuder AG

Address:

Hertzstrasse 4

Heidelberg

69126

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

Ophthalmic surgical procedure kit medicated single-use Ophthalmic surgical procedure kit medicated single-use Class IIa

Ophthalmic surgical procedure kit non-medicated single-use Ophthalmic surgical procedure kit non-medicated single-use Conformity Assessment Certificate Expired Class IIb

Ophthalmic surgical procedure kit non-medicated single-use Ophthalmic surgical procedure kit non-medicated single-use Conformity Assessment Certificate Expired 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
Ophthalmic surgical procedure kit medicated single-use	Ophthalmic surgical procedure kit medicated single-use	Class IIa
Ophthalmic surgical procedure kit non-medicated single-use	Ophthalmic surgical procedure kit non-medicated single-use Conformity Assessment Certificate Expired	Class IIb
Ophthalmic surgical procedure kit non-medicated single-use	Ophthalmic surgical procedure kit non-medicated single-use Conformity Assessment Certificate Expired	Class IIb