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.
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Manufacturer's By Device Automatic-inflation electronic sphygmomanometer portable finger-Automatic-inflation electronic sphygmomanometer portable finger
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
MESI Development of medical devices Ltd.
Leskoškova cesta 11 A
Ljubljana
1000
Slovenia
MESI UK Ltd.
1-3 Manor Road
Chatham
Kent ME4 6AE
England United Kingdom
04/22/2022
24314