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 - Haemotronic S.p.A.

Address:

Via Carreri 16

Mirandola

41037

Italy

Authorised Representative/ UK Responsible Person
Name: NIKKISO UK CO. LTD.
Address:

Unit 2 Ashfields Farm Priors Court Road

Hermitage

RG18 9XY

England United Kingdom

Code/Term Type

Haemodialysis/haemofiltration system component set Haemodialysis/haemofiltration system component set

Haemodialysis blood tubing set single-use Haemodialysis blood tubing set single-use 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
Haemodialysis/haemofiltration system component set	Haemodialysis/haemofiltration system component set
Haemodialysis blood tubing set single-use	Haemodialysis blood tubing set single-use	Class IIa
Haemodialysis blood tubing set single-use	Haemodialysis blood tubing set single-use	Class IIa