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 - BIOMAG Medical

Address:

Karel Hrní – Biomag Chomutice 81

Chomutice

507 53

Czechia

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

Station Yard Station Road

Harrietsham Maidstone

Maidstone

Kent ME17 1JA

England United Kingdom

Code/Term Type

Deep-tissue electromagnetic stimulation system home-use Deep-tissue electromagnetic stimulation system home-use 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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