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 - Durtech Systems Corp.

Address:

3F. No 27 Lane 381 Fude 1st Rd

New Taipei City

New Taipei City

22149

Taiwan

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

Plough Lane

Hereford

HR4 0EL

England United Kingdom

Code/Term Type

Hyperhidrosis iontophoresis system Hyperhidrosis iontophoresis 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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