Extension Tube - FDA Registration 4cf2c35b1833c6aa4144a5a9bcde24a5
Access comprehensive regulatory information for Extension Tube in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4cf2c35b1833c6aa4144a5a9bcde24a5 and manufactured by Nipro (Thailand) Corporation Limited. The device was registered on July 14, 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
4cf2c35b1833c6aa4144a5a9bcde24a5
Extension Tube
FDA ID: 4cf2c35b1833c6aa4144a5a9bcde24a5
Device Classification
Brand Name
Nipro Brand
Registration Information
Analysis ID
4cf2c35b1833c6aa4144a5a9bcde24a5
Registration Date
July 14, 2022
Manufacturer
Authorized Representative

