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 - Villa Sistemi Medicali SpA

Address:

Via delle Azalee 3 20090 Buccinasco (MI)

Buccinasco

20090

Italy

Authorised Representative/ UK Responsible Person
Name: MIS Healthcare Ltd
Address:

Unit 26-27 Capitol Way Capitol Park

London

NW9 0EQ

England United Kingdom

Code/Term Type

Stationary general-purpose fluoroscopic x-ray system analogue Stationary general-purpose fluoroscopic x-ray system analogue Class IIb

Stationary general-purpose fluoroscopic x-ray system digital Stationary general-purpose fluoroscopic x-ray system digital Class IIb

X-ray image intensifier X-ray image intensifier 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
Stationary general-purpose fluoroscopic x-ray system analogue	Stationary general-purpose fluoroscopic x-ray system analogue	Class IIb
Stationary general-purpose fluoroscopic x-ray system digital	Stationary general-purpose fluoroscopic x-ray system digital	Class IIb
X-ray image intensifier	X-ray image intensifier	Class IIb