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 Ultrasound Korea LTD

Address:

9 Sunhwan-ro 214 Beon-gil Jungwon-gu Seongnam-si

Gyeonggi-do

13204

South Korea

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

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

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