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 - Esaote S.p.A.

Address:

Via Enrico Melen 77

Genova

16152

Italy

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Extracorporeal ultrasound imaging transducer hand-held Extracorporeal ultrasound imaging transducer hand-held Class IIa

Rectal/vaginal ultrasound imaging transducer Rectal/vaginal ultrasound imaging transducer Class IIa

Surgical ultrasound imaging transducer Surgical ultrasound imaging transducer Class IIa

Extremity MRI system permanent magnet Extremity MRI system permanent magnet Class IIa

General-purpose ultrasound imaging system General-purpose ultrasound imaging 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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Code/Term		Type
Extracorporeal ultrasound imaging transducer hand-held	Extracorporeal ultrasound imaging transducer hand-held	Class IIa
Rectal/vaginal ultrasound imaging transducer	Rectal/vaginal ultrasound imaging transducer	Class IIa
Surgical ultrasound imaging transducer	Surgical ultrasound imaging transducer	Class IIa
Extremity MRI system permanent magnet	Extremity MRI system permanent magnet	Class IIa
General-purpose ultrasound imaging system	General-purpose ultrasound imaging system	Class IIa