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Absolute Pro & Absolute Pro LL Peripheral Self-Expanding Stent System - FDA Registration c7cba75495cd5e5bba576910948d6fba

Access comprehensive regulatory information for Absolute Pro & Absolute Pro LL Peripheral Self-Expanding Stent System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c7cba75495cd5e5bba576910948d6fba and manufactured by Abbott Vascular. The device was registered on October 21, 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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c7cba75495cd5e5bba576910948d6fba
Absolute Pro & Absolute Pro LL Peripheral Self-Expanding Stent System
FDA ID: c7cba75495cd5e5bba576910948d6fba
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Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
c7cba75495cd5e5bba576910948d6fba
Registration Date
October 21, 2022
Manufacturer
Authorized Representative