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 - advanced fiber tools GmbH

Address:

Bornheimer Str. 4

Mittweida

Saxony D-09648

Germany

Authorised Representative/ UK Responsible Person
Name: OMC MEDICAL Ltd
Address:

Planet House North Heath Lane

Horsham

West Sussex RH12 5QE

United Kingdom

Code/Term Type

Urogenital surgical laser system beam guide single-use Urogenital surgical laser system beam guide single-use Class IIa

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

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
Urogenital surgical laser system beam guide single-use	Urogenital surgical laser system beam guide single-use	Class IIa
General/multiple surgical laser system beam guide single-use	General/multiple surgical laser system beam guide single-use	Class IIa