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 - Sebia

Address:

Parc Technologique Leonard de Vinci CO 8010 Lisses

Evry

91108

France

Authorised Representative/ UK Responsible Person
Name: Sebia (UK) LTD
Address:

River Court Meadows Business Park Station Approach Blackwater

Camberley

Camberley

Surrey GU17 9AB

England United Kingdom

Code/Term Type

Electrophoresis analyser IVD Electrophoresis analyser IVD IVD General

Haemoglobin detection IVD control Haemoglobin detection IVD control IVD General

Multiple haemoglobin subtype IVD kit electrophoresis Multiple haemoglobin subtype IVD kit electrophoresis IVD General

Microplate IVD Microplate 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
Electrophoresis analyser IVD	Electrophoresis analyser IVD	IVD General
Haemoglobin detection IVD control	Haemoglobin detection IVD control	IVD General
Multiple haemoglobin subtype IVD kit electrophoresis	Multiple haemoglobin subtype IVD kit electrophoresis	IVD General
Microplate IVD	Microplate IVD	IVD General