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 - IMEDICOM Co Ltd

Address:

#612 172 LS-ro Grunpo-si

Gyeonggi-do

15807

South Korea

Authorised Representative/ UK Responsible Person
Name: SAFE ORTHOPAEDICS Ltd
Address:

23 Copenhagen Street

London

N1 0JB

England United Kingdom

Code/Term Type

Balloon kyphoplasty kit Balloon kyphoplasty kit 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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