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 - Cardio Sistemas Comercial e Industrial Ltda.

Address:

AV. Paulista 509 10 Andar - Cerqueira Cesar

Sao Paulo

01311-910

Brazil

Authorised Representative/ UK Responsible Person
Name: Patient Guard Limited
Address:

Lancaster House Amy Johnson Way

Blackpool

Lancashire FY42RP

United Kingdom

Code/Term Type

Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Class IIa

Electrocardiographic long-term ambulatory recording analyser application software Electrocardiographic long-term ambulatory recording analyser application software 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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Code/Term		Type
Electrocardiographic ambulatory recorder	Electrocardiographic ambulatory recorder	Class IIa
Electrocardiographic long-term ambulatory recording analyser application software	Electrocardiographic long-term ambulatory recording analyser application software	Class IIa