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 - PROGETTI S.R.L.

Address:

Strada del Rondello 5

TROFARELLO

10028

Italy

Authorised Representative/ UK Responsible Person
Name: Angel Consulting London Ltd
Address:

2 Portman Street

London

W1H 6DU

England United Kingdom

Code/Term Type

Physiologic-monitoring defibrillation system Physiologic-monitoring defibrillation system Class IIb

Electrocardiographic electrode single-use Electrocardiographic electrode single-use Class IIb

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
Physiologic-monitoring defibrillation system	Physiologic-monitoring defibrillation system	Class IIb
Electrocardiographic electrode single-use	Electrocardiographic electrode single-use	Class IIb