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 (UK) LTD

Address:

River Court Meadows Business Park Station Approach Blackwater

Camberley

Camberley

Surrey GU17 9AB

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Electrophoresis analyser IVD Electrophoresis analyser IVD IVD General

Specimen processing instrument IVD Specimen processing instrument IVD IVD General

Clinical laboratory information system application software Clinical laboratory information system application software IVD General

Protein electrophoresis IVD kit electrophoresis Protein electrophoresis IVD kit electrophoresis IVD General

Beta-2-transferrin IVD kit electrophoresis Beta-2-transferrin IVD kit electrophoresis 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
Specimen processing instrument IVD	Specimen processing instrument IVD	IVD General
Clinical laboratory information system application software	Clinical laboratory information system application software	IVD General
Protein electrophoresis IVD kit electrophoresis	Protein electrophoresis IVD kit electrophoresis	IVD General
Beta-2-transferrin IVD kit electrophoresis	Beta-2-transferrin IVD kit electrophoresis	IVD General