FOLEY BALLOON CATHETER (WELLFOLEY) (3 WAY) - FDA Registration c95d8b20c10503336aeed5ab479a248a
Access comprehensive regulatory information for FOLEY BALLOON CATHETER (WELLFOLEY) (3 WAY) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c95d8b20c10503336aeed5ab479a248a and manufactured by Wellmed International Industries Pvt. Ltd. The device was registered on January 18, 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
c95d8b20c10503336aeed5ab479a248a
FOLEY BALLOON CATHETER (WELLFOLEY) (3 WAY)
FDA ID: c95d8b20c10503336aeed5ab479a248a
Device Classification
Brand Name
WELLMED
Registration Information
Analysis ID
c95d8b20c10503336aeed5ab479a248a
Registration Date
January 18, 2022
Manufacturer
Authorized Representative

