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 - Phakos

Address:

62 rue Kleber

Montreuil

93100

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 cryosurgical system electronic Ophthalmic cryosurgical system electronic Class IIb

Laser lens ophthalmic surgical Laser lens ophthalmic surgical Class I

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 cryosurgical system electronic	Ophthalmic cryosurgical system electronic	Class IIb
Laser lens ophthalmic surgical	Laser lens ophthalmic surgical	Class I