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 - SPRINGLIFE MEDICAL B.V

Address:

KAAP DE GOEDE HOOPLAAN 7

Gemeente Utrecht

3526 AR

Netherlands

Authorised Representative/ UK Responsible Person
Name: K A Heritage Ltd
Address:

Wayman House 141 Wickham Road

Croydon

CR0 8TE

England United Kingdom

Code/Term Type

Radio-frequency ablation system Radio-frequency ablation 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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