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 Japan Corporation

Address:

4-7-127 Asahigaoka Hino-Shi

Tokyo

191-8503

Japan

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

CT system application software CT system application software Class IIa

Full-body CT system Full-body CT system Class IIb

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

Surgical ultrasound imaging transducer Surgical ultrasound imaging transducer Class IIa

Rectal/vaginal ultrasound imaging transducer Rectal/vaginal ultrasound imaging transducer 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
CT system application software	CT system application software	Class IIa
Full-body CT system	Full-body CT system	Class IIb
Extracorporeal ultrasound imaging transducer hand-held	Extracorporeal ultrasound imaging transducer hand-held	Class IIa
Surgical ultrasound imaging transducer	Surgical ultrasound imaging transducer	Class IIa
Rectal/vaginal ultrasound imaging transducer	Rectal/vaginal ultrasound imaging transducer	Class IIa