Phototherapy Unit - FDA Registration 02253a8e998aeb3779b9cad4cfc3cd50
Access comprehensive regulatory information for Phototherapy Unit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 02253a8e998aeb3779b9cad4cfc3cd50 and manufactured by Bistos Co., Ltd. The device was registered on April 21, 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
02253a8e998aeb3779b9cad4cfc3cd50
Phototherapy Unit
FDA ID: 02253a8e998aeb3779b9cad4cfc3cd50
Device Classification
Brand Name
BISTOS
Registration Information
Analysis ID
02253a8e998aeb3779b9cad4cfc3cd50
Registration Date
April 21, 2022
Manufacturer
Name
Bistos Co., LtdAuthorized Representative

