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EMBOTRAP III - ARCSA Registration 5bdb2140a0dfb7ae67099a39c6509f11

Access comprehensive regulatory information for EMBOTRAP III in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 5bdb2140a0dfb7ae67099a39c6509f11 and manufactured by ADVANT MEDICAL LTD.. The device was registered on August 26, 2021.

This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.

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ARCSA Official Data
IV
5bdb2140a0dfb7ae67099a39c6509f11
EMBOTRAP III
ARCSA ID: 5bdb2140a0dfb7ae67099a39c6509f11
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
CERENOVUS EMBOTRAPโ„ข III
Commercial Name
Stents, Vascular
Registration Information
Analysis ID
5bdb2140a0dfb7ae67099a39c6509f11
Registration Date
August 26, 2021
Expiration Date
August 26, 2026
Product Use

DESIGNED FOR USE IN THE ANTERIOR AND POSTERIOR NEUROVASCULATURE IN BLOOD VESSELS, SUCH AS THE INTERNAL CAROTID ARTERY, THE M1 AND M2 SEGMENTS OF THE MIDDLE CEREBRAL ARTERY, THE A1 AND A2 SEGMENTS OF THE ANTERIOR CEREBRAL ARTERY, THE BASILAR ARTERY, THE POSTERIOR CEREBRAL ARTERY, AND THE VERTEBRAL ARTERIES.

Manufacturer
Country
IRELAND
Address
PARKMORE BUSINESS PARK WEST
Product Owner
Name
NEURAVI LIMITED
Country
IRELAND
Authorized Representative
Address
AV. CORUร‘A N28-14 Y MANUEL ITURREY, EDIFICIO SANTA FE, OF 11, DIAGONAL A DOMINOS PIZZA
Phone
983350955