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 - NeoDynamics AB

Address:

Lejonvagen 14 SE-181 32

Stockholm

Lidingo SE-181 32

Sweden

Authorised Representative/ UK Responsible Person
Name: MediLife Ltd
Address:

167-169 Great Portland Street

London

W1W5PF

England United Kingdom

Code/Term Type

Biopsy gun handpiece Biopsy gun handpiece 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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