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 - Fujimori Kogyo Co. Ltd.

Address:

1-1-1 Koishikawa Bunkyo-ku

Tokyo

112-0002

Japan

Authorised Representative/ UK Responsible Person
Name: MDSS-UK RP LIMITED
Address:

6 Wilmslow Road Rusholme

Manchester

M14 5TP

England United Kingdom

Code/Term Type

Platelet aggregation analyser IVD Platelet aggregation analyser IVD IVD General

Platelet aggregation study IVD reagent Platelet aggregation study IVD reagent IVD General

Assay container IVD single-use Assay container IVD single-use IVD General

Evacuated blood collection tube IVD anticoagulant Evacuated blood collection tube IVD anticoagulant IVD General

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
Platelet aggregation analyser IVD	Platelet aggregation analyser IVD	IVD General
Platelet aggregation study IVD reagent	Platelet aggregation study IVD reagent	IVD General
Assay container IVD single-use	Assay container IVD single-use	IVD General
Evacuated blood collection tube IVD anticoagulant	Evacuated blood collection tube IVD anticoagulant	IVD General