Phototherapy - FDA Registration d29e354a262cfd1d84c6b54308296110
Access comprehensive regulatory information for Phototherapy in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d29e354a262cfd1d84c6b54308296110 and manufactured by Bistos Co.,Ltd.. The device was registered on November 02, 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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d29e354a262cfd1d84c6b54308296110
Phototherapy
FDA ID: d29e354a262cfd1d84c6b54308296110
Device Classification
Brand Name
bistos BT-400 Phototherapy
Registration Information
Analysis ID
d29e354a262cfd1d84c6b54308296110
Registration Date
November 02, 2021
Manufacturer
Name
Bistos Co.,Ltd.Authorized Representative

