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 Medical Systems Information Technologies INC

Address:

8200 W Tower Avenue

Milwaukee

53223

United States

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

Electrocardiograph professional multichannel Electrocardiograph professional multichannel Class IIa

Electrocardiographic long-term ambulatory recording analyser Electrocardiographic long-term ambulatory recording analyser Class IIa

Cardiology information system application software Cardiology information system application software Class IIa

Electrocardiographic lead set reusable Electrocardiographic lead set reusable Class IIa

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
Electrocardiograph professional multichannel	Electrocardiograph professional multichannel	Class IIa
Electrocardiographic long-term ambulatory recording analyser	Electrocardiographic long-term ambulatory recording analyser	Class IIa
Cardiology information system application software	Cardiology information system application software	Class IIa
Electrocardiographic lead set reusable	Electrocardiographic lead set reusable	Class IIa