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 - Saalmann medical GmbH & Co. KG

Address:

Südbahnstraße 34

Bad Oeynhausen

32547

Germany

Authorised Representative/ UK Responsible Person
Name: Memory Business Systems ltd
Address:

Onega House 112 Main Road

Sidcup London

London

DA14 6NE

England United Kingdom

Code/Term Type

Ultraviolet phototherapy unit home-use Ultraviolet phototherapy unit home-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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