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

Image display unit colour Image display unit colour Class IIb

Patient monitoring system module rack Patient monitoring system module rack Class IIb

Breathing circuit gas-flow sensor reusable Breathing circuit gas-flow sensor reusable Class IIa

Patient monitoring system module interfacing Patient monitoring system module interfacing Class IIb

Patient monitoring system module cardiac output Patient monitoring system module cardiac output 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
Image display unit colour	Image display unit colour	Class IIb
Patient monitoring system module rack	Patient monitoring system module rack	Class IIb
Breathing circuit gas-flow sensor reusable	Breathing circuit gas-flow sensor reusable	Class IIa
Patient monitoring system module interfacing	Patient monitoring system module interfacing	Class IIb
Patient monitoring system module cardiac output	Patient monitoring system module cardiac output	Class IIb