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 - Derungs Licht AG

Address:

Hofmattstrasse 12

Gossau

9200

Switzerland

Authorised Representative/ UK Responsible Person
Name: International Associates Limited
Address:

38 Queen Street

Glasgow

G1 3DX

Scotland United Kingdom

Code/Term Type

Mobile examination/treatment room light Mobile examination/treatment room light Class I

Fixed examination/treatment room light Fixed examination/treatment room light Class I

Blue light radiometer Blue light radiometer 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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Code/Term		Type
Mobile examination/treatment room light	Mobile examination/treatment room light	Class I
Fixed examination/treatment room light	Fixed examination/treatment room light	Class I
Blue light radiometer	Blue light radiometer	Class I