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Penumbra Delivery Microcatheters - ARCSA Registration 504e8036f1f50d2876d2aa55019dabee

Access comprehensive regulatory information for Penumbra Delivery Microcatheters in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 504e8036f1f50d2876d2aa55019dabee 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
504e8036f1f50d2876d2aa55019dabee
Penumbra Delivery Microcatheters
ARCSA ID: 504e8036f1f50d2876d2aa55019dabee
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
PENUMBRA
Commercial Name
Catheters
Registration Information
Analysis ID
504e8036f1f50d2876d2aa55019dabee
Registration Date
January 06, 2023
Expiration Date
January 06, 2028
Product Use

PENUMBRA IMPLANTATION MICROCATHETERS ARE INDICATED TO HELP THE IMPLANTATION OF DIAGNOSTIC AGENTS, AS A CONTRAST MEDIUM, AND THERAPEUTIC AGENTS, SUCH AS OCCLUSION COILS, IN THE PERIPHERAL VASCULATURE AND NEUROVASCULATURE.

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