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 - Teckel Medical S.L.

Address:

Calle Sant Antoni Maria Claret 167 Pabellon Sant Manuel

Barcelona

08025

Spain

Authorised Representative/ UK Responsible Person
Name: Regulis Consulting Limited
Address:

The Pool Innovation Centre Trevenson Road

Redruth

Cornwall TR15 3PL

England United Kingdom

Code/Term Type

Clinical management support software Clinical management support software Class I

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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