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 - A&D Company Limited

Address:

1-243 Asahi Kitamoto-shi

Saitama-ken

Tokyo

364-8585

Japan

Authorised Representative/ UK Responsible Person
Name: A&D Instruments Ltd
Address:

24-26 BLACKLANDS WAY ABINGDON BUSINESS PARK

ABINGDON

OXFORDSHIRE OX14 1DY

England United Kingdom

Code/Term Type

Manual-inflation electronic sphygmomanometer portable Manual-inflation electronic sphygmomanometer portable Class IIa

Blood pressure cuff single-use Blood pressure cuff single-use Class I

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

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
Manual-inflation electronic sphygmomanometer portable	Manual-inflation electronic sphygmomanometer portable	Class IIa
Blood pressure cuff single-use	Blood pressure cuff single-use	Class I
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