Double J Stent (Both End Open) - FDA Registration 06353cdf0a9b9793a705b755db661df7
Access comprehensive regulatory information for Double J Stent (Both End Open) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 06353cdf0a9b9793a705b755db661df7 and manufactured by Biorad Medisys Pvt. Ltd.. The device was registered on July 26, 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
06353cdf0a9b9793a705b755db661df7
Double J Stent (Both End Open)
FDA ID: 06353cdf0a9b9793a705b755db661df7
Device Classification
Brand Name
INDOVASIVE
Registration Information
Analysis ID
06353cdf0a9b9793a705b755db661df7
Registration Date
July 26, 2022
Manufacturer
Authorized Representative

