Exilis Ultra 360 (Exilis system with Large and XP applicators) - FDA Registration e608f1c892c432ca2b17d2ff558967ff
Access comprehensive regulatory information for Exilis Ultra 360 (Exilis system with Large and XP applicators) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e608f1c892c432ca2b17d2ff558967ff and manufactured by BTL Industries. The device was registered on June 02, 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
e608f1c892c432ca2b17d2ff558967ff
Exilis Ultra 360 (Exilis system with Large and XP applicators)
FDA ID: e608f1c892c432ca2b17d2ff558967ff
Device Classification
Brand Name
BTL
Registration Information
Analysis ID
e608f1c892c432ca2b17d2ff558967ff
Registration Date
June 02, 2022
Manufacturer
Name
BTL IndustriesAuthorized Representative

