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 - Tuylek s.l.

Address:

La Pujada 19 19 pol. Ind. Els garrofers

Vilassar de Mar

Barcelona 08340

Spain

Authorised Representative/ UK Responsible Person
Name: Venturama Limited
Address:

Falconer Stewart Accountants 248 Upper Newtownards Road

Belfast

Antrim BT4 3EU

Northern Ireland United Kingdom

Code/Term Type

Automatic-inflation electronic sphygmomanometer non-portable Automatic-inflation electronic sphygmomanometer non-portable 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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