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 - INNOVEX MEDICAL CO. LTD.

Address:

1F and East 2F Building 7 No.150 Cailun Road

Pilot Free Trade Zone

Shanghai

201210

China

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

Flexible ureteral sheath/fibreoptic telescope Flexible ureteral sheath/fibreoptic telescope Class IIa

Polymeric ureteral stent Polymeric ureteral stent Class IIa

Biliary/urinary stone retrieval basket single-use Biliary/urinary stone retrieval basket single-use Class IIa

Gastro-urological guidewire single-use Gastro-urological guidewire single-use Class IIa

Urethral dilatation catheter non-medicated Urethral dilatation catheter non-medicated 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
Flexible ureteral sheath/fibreoptic telescope	Flexible ureteral sheath/fibreoptic telescope	Class IIa
Polymeric ureteral stent	Polymeric ureteral stent	Class IIa
Biliary/urinary stone retrieval basket single-use	Biliary/urinary stone retrieval basket single-use	Class IIa
Gastro-urological guidewire single-use	Gastro-urological guidewire single-use	Class IIa
Urethral dilatation catheter non-medicated	Urethral dilatation catheter non-medicated	Class IIa