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 - ZHANJIANG STAR ENTERPRISE CO. LTD.

Address:

No. 1 West Jinhua Road Mazhang District

Zhanjiang

Guangdong 524094

China

Authorised Representative/ UK Responsible Person
Name: Conjoint Export Services (SA) Ltd.
Address:

92 Brinkley Road

Worcester Park

Surrey KT4 8JF

England United Kingdom

Code/Term Type

Indwelling urethral catheterization kit adult Indwelling urethral catheterization kit adult Class IIa

Indwelling urethral drainage balloon catheter non-antimicrobial Indwelling urethral drainage balloon catheter non-antimicrobial Class IIa

Basic endotracheal tube single-use Basic endotracheal tube single-use Class IIa

Reinforced endotracheal tube single-use Reinforced endotracheal tube 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
Indwelling urethral catheterization kit adult	Indwelling urethral catheterization kit adult	Class IIa
Indwelling urethral drainage balloon catheter non-antimicrobial	Indwelling urethral drainage balloon catheter non-antimicrobial	Class IIa
Basic endotracheal tube single-use	Basic endotracheal tube single-use	Class IIa
Reinforced endotracheal tube single-use	Reinforced endotracheal tube single-use	Class IIa