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Penumbra Coil System / Ruby® Coil System Standard - ARCSA Registration b017e729a317cf931f31a4041aeb36e4

Access comprehensive regulatory information for Penumbra Coil System / Ruby® Coil System Standard in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID b017e729a317cf931f31a4041aeb36e4 and manufactured by PENUMBRA, INC.. The device was registered on December 21, 2022.

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
b017e729a317cf931f31a4041aeb36e4
Penumbra Coil System / Ruby® Coil System Standard
ARCSA ID: b017e729a317cf931f31a4041aeb36e4
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
PENUMBRA
Commercial Name
Non-neurovascular embolization spiral
Registration Information
Analysis ID
b017e729a317cf931f31a4041aeb36e4
Registration Date
December 21, 2022
Expiration Date
December 21, 2027
Product Use

THE RUBY COIL SYSTEM IS INDICATED FOR ARTERIAL AND VENOUS EMBOLIZATIONS IN THE PERIPHERAL VASCULATURE.

Manufacturer
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, VIA TANDA
Phone
22899256