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 - Dornier MedTech America Inc.

Address:

1155 Roberts Boulevard

Kennesaw

Georgia 30144

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

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

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