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

Back to MHRA

Manufacturer's Devices - F.M. S.p.A.

Address:

Via Farini 65 bis

Cigliano

13043

Italy

Authorised Representative/ UK Responsible Person
Name: MDQ Services Ltd
Address:

Flat 81 Seacon Tower 5 Hutching’s Street

London

England E14 8JX

England United Kingdom

Code/Term Type

Blood transfer set Blood transfer set Class IIa

Catheter injection port Catheter injection port Class IIa

Basic intravenous administration set noninvasive Basic intravenous administration set noninvasive Class IIa

Haemodialysis blood tubing set single-use Haemodialysis blood tubing set single-use 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
Blood transfer set	Blood transfer set	Class IIa
Catheter injection port	Catheter injection port	Class IIa
Basic intravenous administration set noninvasive	Basic intravenous administration set noninvasive	Class IIa
Haemodialysis blood tubing set single-use	Haemodialysis blood tubing set single-use	Class IIa