ichroma Myoglobin Neo - FDA Registration fddede10585921ff3461607e23aeb8ee
Access comprehensive regulatory information for ichroma Myoglobin Neo in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fddede10585921ff3461607e23aeb8ee and manufactured by Boditech Med Inc. The device was registered on November 10, 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
fddede10585921ff3461607e23aeb8ee
ichroma Myoglobin Neo
FDA ID: fddede10585921ff3461607e23aeb8ee
Device Classification
Brand Name
ichroma
Registration Information
Analysis ID
fddede10585921ff3461607e23aeb8ee
Registration Date
November 10, 2022
Manufacturer
Name
Boditech Med IncAuthorized Representative

