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 Austria GmbH & CO OG

Address:

15 Tiefenbach

Zipf

4871

Austria

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

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

Rectal/vaginal ultrasound imaging transducer Rectal/vaginal ultrasound imaging transducer Class IIa

Ultrasound imaging system operation software Ultrasound imaging system operation software Class IIa

Ultrasound imaging system operation software Ultrasound imaging system operation 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
Extracorporeal ultrasound imaging transducer hand-held	Extracorporeal ultrasound imaging transducer hand-held	Class IIa
Rectal/vaginal ultrasound imaging transducer	Rectal/vaginal ultrasound imaging transducer	Class IIa
Ultrasound imaging system operation software	Ultrasound imaging system operation software	Class IIa
Ultrasound imaging system operation software	Ultrasound imaging system operation software	Class IIa