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 - Candela Corporation

Address:

251 Locke Drive

Marlborough

Massachusetts 01752

United States

Authorised Representative/ UK Responsible Person
Name: UKCApartner4U Limited
Address:

7 CAMPION WAY

BINGHAM NOTTINGHAM

NG13 8 TR

England United Kingdom

Code/Term Type

Multi-modality skin surface treatment system Multi-modality skin surface treatment system Conformity Assessment Certificate Expired Class IIb

Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Class IIb

Dermatological solid-state laser system Dermatological solid-state laser system Class IIb

Dermatological dye laser system Dermatological dye 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
Multi-modality skin surface treatment system	Multi-modality skin surface treatment system Conformity Assessment Certificate Expired	Class IIb
Dermatological frequency-doubled solid-state laser system	Dermatological frequency-doubled solid-state laser system	Class IIb
Dermatological solid-state laser system	Dermatological solid-state laser system	Class IIb
Dermatological dye laser system	Dermatological dye laser system	Class IIb