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 - Leja Products B.V.

Address:

Luzernestraat 10

Nieuw Vennep

Haarlemmermeer

Provincie Noord-Holland 2153 GN

Netherlands

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

Bicester Innovation Centre Commerce House Telford Road

Bicester

Oxfordshire OX26 4LD

England United Kingdom

Code/Term Type

General specimen microscopy slide IVD single-use General specimen microscopy slide IVD single-use Class A

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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