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 - HS DOMS GmbH

Address:

LANGENSCHADER STRASSE 67

D-07318 SAALFELD

EU

Germany

Authorised Representative/ UK Responsible Person
Name: HAAG STREIT UK LTD
Address:

Unit A Cartel Business Estate

EDINBURGH WAY

HARLOW

ESSEX CM20 2TT

United Kingdom

Code/Term Type

Ophthalmic instrument table line-powered Ophthalmic instrument table line-powered 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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