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 - GE Healthcare Finland Oy

Address:

Kuortaneenkatu 2

Helsinki

FI-00510

Finland

Authorised Representative/ UK Responsible Person
Name: GE Medical Systems Limited
Address:

Pollards Wood Nightingales Lane Buckinghamshire

Chalfont St Giles

HP8 4SP

England United Kingdom

Code/Term Type

Analytical scalp electrode single-use Analytical scalp electrode single-use Class IIb

Pulse oximeter line-powered Pulse oximeter line-powered Class IIb

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
Analytical scalp electrode single-use	Analytical scalp electrode single-use	Class IIb
Pulse oximeter line-powered	Pulse oximeter line-powered	Class IIb