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POD (PENUMBRA OCCLUSION DEVICE) SYSTEM POD - ARCSA Registration be6198c0ba5e7c4c83612da297768a99

Access comprehensive regulatory information for POD (PENUMBRA OCCLUSION DEVICE) SYSTEM POD in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID be6198c0ba5e7c4c83612da297768a99 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
be6198c0ba5e7c4c83612da297768a99
POD (PENUMBRA OCCLUSION DEVICE) SYSTEM POD
ARCSA ID: be6198c0ba5e7c4c83612da297768a99
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
PENUMBRA
Commercial Name
OCCLUDERS, VASCULAR, FOR INTRAVASCULAR EMBOLIZACION
Registration Information
Analysis ID
be6198c0ba5e7c4c83612da297768a99
Registration Date
May 10, 2019
Expiration Date
May 10, 2024
Product Use

IT IS USED FOR ENDOVASCULAR EMBOLIZATION OF INTRACRANIAL ANEURYSMS, OTHER NEUROVASCULAR ABNORMALITIES SUCH AS ARTERIOVENOUS MALFORMATIONS AND ARTERIOVENOUS FISTULAS, AND FOR ARTERIAL AND VENOUS EMBOLIZATIONS IN THE PERIPHERAL VASCULATURE.

Manufacturer
Country
UNITED STATES
Address
1351 HARBOR BAY PARKWAY, ALAMEDA, CA, 94502 USA
Product Owner
Name
HEALTH SPHERE LLC
Country
UNITED STATES
Authorized Representative
Address
AV DE LOS SHYRIS N9-38 AND BELGICA STREET
Phone
23800917