Supera Peripheral Stent System - FDA Registration 778db373c06cc3149f730c4f45169b28
Access comprehensive regulatory information for Supera Peripheral Stent System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 778db373c06cc3149f730c4f45169b28 and manufactured by Abbott Vascular. The device was registered on September 28, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
778db373c06cc3149f730c4f45169b28
Supera Peripheral Stent System
FDA ID: 778db373c06cc3149f730c4f45169b28
Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
778db373c06cc3149f730c4f45169b28
Registration Date
September 28, 2022
Manufacturer
Name
Abbott VascularAuthorized Representative

