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 - Bosch + Sohn GmbH u. Co KG

Address:

Bahnhofstrabe 64

Jungingen

D-72417

Germany

Authorised Representative/ UK Responsible Person
Name: Albert Waeschle Ltd
Address:

11 Balena Close Creekmoor

Poole

Dorset BH17 7DB

United Kingdom

Code/Term Type

Mechanical stethoscope Mechanical stethoscope Class I

Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Class I

Infrared patient thermometer ear Infrared patient thermometer ear Class IIa

Blood pressure cuff reusable Blood pressure cuff reusable Class I

Automatic-inflation electronic sphygmomanometer portable arm/wrist Automatic-inflation electronic sphygmomanometer portable arm/wrist Class IIa

Liquid-crystal patient thermometer reusable Liquid-crystal patient thermometer 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
Mechanical stethoscope	Mechanical stethoscope	Class I
Aneroid manual sphygmomanometer	Aneroid manual sphygmomanometer	Class I
Infrared patient thermometer ear	Infrared patient thermometer ear	Class IIa
Blood pressure cuff reusable	Blood pressure cuff reusable	Class I
Automatic-inflation electronic sphygmomanometer portable arm/wrist	Automatic-inflation electronic sphygmomanometer portable arm/wrist	Class IIa
Liquid-crystal patient thermometer reusable	Liquid-crystal patient thermometer reusable	Class IIa