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 - Yvsolab NV

Address:

Veedijk 33

BE-2300 Turnhout

BE-2300

Belgium

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

ANATOPATH LTD London Road

The Haven

Saxmundham

Suffolk IP17 3QL

England United Kingdom

Code/Term Type

Neutral buffered formalin IVD Neutral buffered formalin 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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