Ultrasonic Generator - FDA Registration b214202c7e3e3074896d5636effe965d
Access comprehensive regulatory information for Ultrasonic Generator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b214202c7e3e3074896d5636effe965d and manufactured by Aomori Olympus Co., Ltd. The device was registered on November 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
b214202c7e3e3074896d5636effe965d
Ultrasonic Generator
FDA ID: b214202c7e3e3074896d5636effe965d
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
b214202c7e3e3074896d5636effe965d
Registration Date
November 28, 2022
Manufacturer
Authorized Representative

