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 - Quantel Medical Ltd

Address:

11 rue du Bois Joli CS 40015

Cedex

Cournon d’-Auvergne 63808

France

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 ultrasound imaging system Ophthalmic ultrasound imaging system Conformity Assessment Certificate Expired Class IIa

Intense pulsed light dry eye therapy unit Intense pulsed light dry eye therapy unit Class IIb

Ophthalmic solid-state laser system Ophthalmic ultrasound imaging system Class IIb

Ophthalmic solid-state laser system Ophthalmic solid-state laser system 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 ultrasound imaging system	Ophthalmic ultrasound imaging system Conformity Assessment Certificate Expired	Class IIa
Intense pulsed light dry eye therapy unit	Intense pulsed light dry eye therapy unit	Class IIb
Ophthalmic solid-state laser system	Ophthalmic ultrasound imaging system	Class IIb
Ophthalmic solid-state laser system	Ophthalmic solid-state laser system	Class IIb