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 - FUJIFILM Wako Pure Chemical Corporation

Address:

1-2 Doshomachi 3-chome

1-2 Doshomachi 3-chome

Osaka

Chuo-ku 540-8605

Japan

Authorised Representative/ UK Responsible Person
Name: Fujifilm UK Limited
Address:

Fujifilm House Whitbread Way

Bedford

MK42 0ZE

England United Kingdom

Code/Term Type

13-Beta-D-glucan IVD kit nephelometry/turbidimetry 13-Beta-D-glucan IVD kit nephelometry/turbidimetry IVD General

Nephelometry/turbidimetry analyser IVD manual Nephelometry/turbidimetry analyser IVD manual 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
13-Beta-D-glucan IVD kit nephelometry/turbidimetry	13-Beta-D-glucan IVD kit nephelometry/turbidimetry	IVD General
Nephelometry/turbidimetry analyser IVD manual	Nephelometry/turbidimetry analyser IVD manual	IVD General