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 - DMS

Address:

290 Kingsbury Grade #3 Stateline

Douglas

NV 89449

United States

Authorised Representative/ UK Responsible Person
Name: Numed Holdings Ltd t/a Numed Healthcare
Address:

Alliance House Roman Ridge Road

Sheffield

S9 1GB

England United Kingdom

Code/Term Type

Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Class IIa

Electrocardiographic long-term ambulatory recording analyser Electrocardiographic long-term ambulatory recording analyser 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	Electrocardiographic long-term ambulatory recording analyser	Class IIa