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 Irvine Scientific Inc

Address:

2511 Daimler Street

Santa Ana

California 92705

United States

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

Fujifilm House Whitbread Way

Bedford

MK42 0ZE

England United Kingdom

Code/Term Type

IVF medium IVF medium Class IIb

Cell culture medium IVD Cell culture medium IVD IVD General

Cell culture medium IVD Cell culture medium IVD Class III

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
IVF medium	IVF medium	Class IIb
Cell culture medium IVD	Cell culture medium IVD	IVD General
Cell culture medium IVD	Cell culture medium IVD	Class III