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 - DO-ALL Corp.

Address:

30 Magokdong-ro

Seoul

Gangseo-gu 157-870

South Korea

Authorised Representative/ UK Responsible Person
Name: 4T Medical Ltd
Address:

G12 Blenheim House Cambridge Innovation Park Denny End Road

Waterbeach Cambridge

Cambridge

CB25 9GL

England United Kingdom

Code/Term Type

Multiple-pronged submucosal injection needle Multiple-pronged submucosal injection needle 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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