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 - PIOLAX MEDICAL DEVICES INC.

Address:

2265-3 Kamiyabe-cho Totsuka-ku

Yokohama-shi Kanagawa

245-0053,

Japan

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

Peripheral vascular guidewire manual Peripheral vascular guidewire manual Class IIa

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

Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter 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
Peripheral vascular guidewire manual	Peripheral vascular guidewire manual	Class IIa
Gastro-urological guidewire single-use	Gastro-urological guidewire single-use	Class IIa
Peripheral vascular intervention infusion catheter	Peripheral vascular intervention infusion catheter	Class IIa