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 - NeuroVasc Technologies Inc.

Address:

3 Jenner Ste. 100

Irvine

California 92618

United States

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

Thrombectomy suction catheter Thrombectomy suction catheter Class III

Vascular guide-catheter single-use Vascular guide-catheter single-use Class III

Vascular guide-catheter single-use Vascular guide-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
Thrombectomy suction catheter	Thrombectomy suction catheter	Class III
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class III
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class III