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 - MICROPORT NEUROTECH (SHANGHAI) Co. LTD.

Address:

BUILDING No. 16 222 GUANGDAN ROAD

PUDONG NEW DISTRICT

SHANGHAI

201318

China

Authorised Representative/ UK Responsible Person
Name: European Device Solutions Ltd
Address:

15 COANWOOD DRIVE Whitley Bay

WHITLEY BAY

TYNE AND WEAR NE25 9GB

England United Kingdom

Code/Term Type

Vascular implant detacher electronic single-use Vascular implant detacher electronic single-use Class IIa

Neurovascular embolization coil Neurovascular embolization coil 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
Vascular implant detacher electronic single-use	Vascular implant detacher electronic single-use	Class IIa
Neurovascular embolization coil	Neurovascular embolization coil	Class III