Synthetic Hemodialyzer - FDA Registration dcfbc0fb97496fbb27bbd8fa06c351ef
Access comprehensive regulatory information for Synthetic Hemodialyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dcfbc0fb97496fbb27bbd8fa06c351ef and manufactured by Nipro Corporation Odate Factory. The device was registered on November 25, 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
dcfbc0fb97496fbb27bbd8fa06c351ef
Synthetic Hemodialyzer
FDA ID: dcfbc0fb97496fbb27bbd8fa06c351ef
Device Classification
Brand Name
Nipro
Registration Information
Analysis ID
dcfbc0fb97496fbb27bbd8fa06c351ef
Registration Date
November 25, 2022
Manufacturer
Authorized Representative

