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 - Togo Medikit Co. Ltd.

Address:

17148-6 Aza Kamekawa Oaza Hichiya

Hyuga

883-0062

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 intervention infusion catheter Peripheral vascular intervention infusion catheter Class IIa

Haemodialysis needle Haemodialysis needle Class IIa

Vascular catheter introduction set nonimplantable Vascular catheter introduction set nonimplantable Class IIa

Angiographic catheter single-use Angiographic catheter single-use Class IIa

Angiographic catheter single-use Angiographic catheter single-use Class III

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 intervention infusion catheter	Peripheral vascular intervention infusion catheter	Class IIa
Haemodialysis needle	Haemodialysis needle	Class IIa
Vascular catheter introduction set nonimplantable	Vascular catheter introduction set nonimplantable	Class IIa
Angiographic catheter single-use	Angiographic catheter single-use	Class IIa
Angiographic catheter single-use	Angiographic catheter single-use	Class III