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 - miha bodytec GmbH

Address:

Siemensstraße 1

Gersthofen

86368

Germany

Authorised Representative/ UK Responsible Person
Name: miha bodytec ems UK Ltd.
Address:

Suite 1 3rd Floor

11-12 St. James's Square

London

SW1Y4LB

England United Kingdom

Code/Term Type

Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system 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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