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 - Nihon Kohden Firenze S.r.l.

Address:

Via Torta 72/74

Sesto Fiorentino Firenze

FI Florence 50019

Italy

Authorised Representative/ UK Responsible Person
Name: NIHONKOHDEN UK LTD
Address:

Unit 3 Heyworth Business Park Old Portsmouth Road Peasmarsh

GUILDFORD

GUILDFORD

Surrey GU3 1AF

England United Kingdom

Code/Term Type

Buffered sample diluent IVD Buffered sample diluent IVD IVD General

Wash/cleaning solution IVD automated/semi-automated system Wash/cleaning solution IVD automated/semi-automated system IVD General

Blood cell lysis reagent IVD Blood cell lysis reagent IVD 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
Buffered sample diluent IVD	Buffered sample diluent IVD	IVD General
Wash/cleaning solution IVD automated/semi-automated system	Wash/cleaning solution IVD automated/semi-automated system	IVD General
Blood cell lysis reagent IVD	Blood cell lysis reagent IVD	IVD General