Myanmar FDA registration fc330fb1d2a4402f356419ad0242dde7
Endopyelotomy Stent
Device classification
- Brand Name
- INDOVASIVE
Registration information
- Analysis ID
- fc330fb1d2a4402f356419ad0242dde7
- Registration Date
- July 26, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Endopyelotomy Stent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fc330fb1d2a4402f356419ad0242dde7 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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