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INDIGO Aspiration System - ARCSA Registration eeb4bd857fb3fc40db4ebe90cd49f8e9

Access comprehensive regulatory information for INDIGO Aspiration System in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID eeb4bd857fb3fc40db4ebe90cd49f8e9 and manufactured by PENUMBRA, INC.. The device was registered on January 06, 2023.

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
eeb4bd857fb3fc40db4ebe90cd49f8e9
INDIGO Aspiration System
ARCSA ID: eeb4bd857fb3fc40db4ebe90cd49f8e9
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
PENUMBRA
Commercial Name
Catheters
Registration Information
Analysis ID
eeb4bd857fb3fc40db4ebe90cd49f8e9
Registration Date
January 06, 2023
Expiration Date
January 06, 2028
Product Use

THE INDIGO ASPIRATION SYSTEM IS DESIGNED TO REMOVE THROMBI FROM THE VASCULATURE BY CONTINUOUS ASPIRATION. THE INDIGO ASPIRATION CATHETER IT DIRECTS THE ASPIRATION OF THE PUMP DIRECTLY TO THE THROMBUS.

Manufacturer
City
ALAMEDA, CA 94502
Country
UNITED STATES
Address
ONE PENUMBRA PLACE
Product Owner
Name
PENUMBRA, INC.
Country
UNITED STATES
Authorized Representative
Address
AV. EUGENIO ESPEJO, CONJUNTO VISTALBA S/N, Y PASAJE S17, VIA TANDA
Phone
22899256