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 Ultrasound and Primary Care Diagnostics LLC

Address:

9900 Innovation Drive

Wauwatosa

53226

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

General-purpose ultrasound imaging system General-purpose ultrasound imaging system Class IIa

Breast ultrasound imaging system Breast ultrasound imaging system Class IIa

Extracorporeal ultrasound imaging transducer hand-held Extracorporeal ultrasound imaging transducer hand-held Class IIa

Radiology PACS software Radiology PACS software 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
General-purpose ultrasound imaging system	General-purpose ultrasound imaging system	Class IIa
Breast ultrasound imaging system	Breast ultrasound imaging system	Class IIa
Extracorporeal ultrasound imaging transducer hand-held	Extracorporeal ultrasound imaging transducer hand-held	Class IIa
Radiology PACS software	Radiology PACS software	Class IIa