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 - Bain Medical Equipment (Guangzhou) Co Ltd

Address:

No 10 Juncheng Road Eastern Area

Economic and Technological Development District

Guangzhou

510760

China

Authorised Representative/ UK Responsible Person
Name: Medimap Ltd
Address:

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Haemodialysis concentrate Haemodialysis concentrate Class IIb

Hollow-fibre haemodialysis dialyser single-use Hollow-fibre haemodialysis dialyser single-use Class IIb

Haemodialysis needle Haemodialysis needle 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 concentrate	Haemodialysis concentrate	Class IIb
Hollow-fibre haemodialysis dialyser single-use	Hollow-fibre haemodialysis dialyser single-use	Class IIb
Haemodialysis needle	Haemodialysis needle	Class IIa
Haemodialysis blood tubing set single-use	Haemodialysis blood tubing set single-use	Class IIa