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 - QT Medical Inc

Address:

1360 Valley Vista Drive Suite 203

Diamond Bar

California 91765

United States

Authorised Representative/ UK Responsible Person
Name: Medimap Ltd
Address:

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Electrocardiograph home-use Electrocardiograph home-use Class IIa

Electrocardiographic electrode single-use Electrocardiographic electrode single-use 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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Code/Term		Type
Electrocardiograph home-use	Electrocardiograph home-use	Class IIa
Electrocardiographic electrode single-use	Electrocardiographic electrode single-use	Class I