Refill solution for ISE Electrode - FDA Registration bfa4de3e94f4d511cc6eaaf2e4b152f1
Access comprehensive regulatory information for Refill solution for ISE Electrode in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID bfa4de3e94f4d511cc6eaaf2e4b152f1 and manufactured by Meizhou Cornley Hi-Tech Co., Ltd.. The device was registered on December 21, 2021.
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
bfa4de3e94f4d511cc6eaaf2e4b152f1
Refill solution for ISE Electrode
FDA ID: bfa4de3e94f4d511cc6eaaf2e4b152f1
Device Classification
Brand Name
Cornley
Registration Information
Analysis ID
bfa4de3e94f4d511cc6eaaf2e4b152f1
Registration Date
December 21, 2021
Manufacturer
Authorized Representative

