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 - Medisana GmbH

Address:

Carl-Schurz-Str.2

Neuss

41460

Germany

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Infrared patient thermometer ear Infrared patient thermometer ear Class IIa

Pulse oximeter Pulse oximeter Class IIa

Infrared patient thermometer skin Infrared patient thermometer skin Class IIa

Benchtop nebulizer non-heated Benchtop nebulizer non-heated Class IIa

Automatic-inflation electronic sphygmomanometer portable arm/wrist Automatic-inflation electronic sphygmomanometer portable arm/wrist 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
Infrared patient thermometer ear	Infrared patient thermometer ear	Class IIa
Pulse oximeter	Pulse oximeter	Class IIa
Infrared patient thermometer skin	Infrared patient thermometer skin	Class IIa
Benchtop nebulizer non-heated	Benchtop nebulizer non-heated	Class IIa
Automatic-inflation electronic sphygmomanometer portable arm/wrist	Automatic-inflation electronic sphygmomanometer portable arm/wrist	Class IIa