PENUMBRA COIL SYSTEM/ RUBY COIL SYSTEM - ARCSA Registration 77fac1aab833002365eba2d80463f2a5
Access comprehensive regulatory information for PENUMBRA COIL SYSTEM/ RUBY COIL SYSTEM in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 77fac1aab833002365eba2d80463f2a5 and manufactured by PENUMBRA, INC.. The device was registered on May 10, 2019.
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
77fac1aab833002365eba2d80463f2a5
PENUMBRA COIL SYSTEM/ RUBY COIL SYSTEM
ARCSA ID: 77fac1aab833002365eba2d80463f2a5
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
PENUMBRA
Commercial Name
OCCLUDERS, VASCULAR, FOR INTRAVASCULAR EMBOLIZACION
Registration Information
Analysis ID
77fac1aab833002365eba2d80463f2a5
Registration Date
May 10, 2019
Expiration Date
May 10, 2024
Product Use
USED FOR ARTERIAL AND VENOUS EMBOLIZATIONS IN THE PERIPHERAL VASCULATURE
Manufacturer
Product Owner
Name
HEALTH SPHERE LLC
Country
UNITED STATES
Authorized Representative