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 - Angiodroid SpA

Address:

Via Speranza 35

San Lazzaro di Savena

BO 40068

Italy

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Angiography contrast medium injection system line-powered mobile Angiography contrast medium injection system line-powered mobile Class IIb

Intravenous administration tubing extension set Intravenous administration tubing extension set Class IIa

Angiography kit Angiography kit 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
Angiography contrast medium injection system line-powered mobile	Angiography contrast medium injection system line-powered mobile	Class IIb
Intravenous administration tubing extension set	Intravenous administration tubing extension set	Class IIa
Angiography kit	Angiography kit	Class IIa