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 - CeramOptec GmbH

Address:

Siemensstraße 44; D-53121

Bonn

D-53121

Germany

Authorised Representative/ UK Responsible Person
Name: Promed Ltd
Address:

Hollickwood Rectory Road

Bluntisham

Huntingdon

Cambridgeshire PE28 3LN

England United Kingdom

Code/Term Type

General/multiple surgical diode laser system General/multiple surgical diode laser system Class IIb

General/multiple surgical laser system beam guide single-use General/multiple surgical laser system beam guide single-use 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
General/multiple surgical diode laser system	General/multiple surgical diode laser system	Class IIb
General/multiple surgical laser system beam guide single-use	General/multiple surgical laser system beam guide single-use	Class IIb