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 LLC

Address:

3000 N Grandview Blvd

Waukesha

53188

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

Full-body MRI system superconducting magnet Full-body MRI system superconducting magnet Class IIa

MRI system coil radio-frequency MRI system coil radio-frequency Class I

MRI system synchronizer MRI system synchronizer Class I

MRI image enhancement padding MRI image enhancement padding Class I

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

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
Full-body MRI system superconducting magnet	Full-body MRI system superconducting magnet	Class IIa
MRI system coil radio-frequency	MRI system coil radio-frequency	Class I
MRI system synchronizer	MRI system synchronizer	Class I
MRI image enhancement padding	MRI image enhancement padding	Class I
Full-body CT system	Full-body CT system	Class IIb