Neonatal Phototherapy Unit - FDA Registration b2d1f20bb1ea903617eee496d58d20aa
Access comprehensive regulatory information for Neonatal Phototherapy Unit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b2d1f20bb1ea903617eee496d58d20aa and manufactured by Bistos Co., Ltd.. The device was registered on September 28, 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
b2d1f20bb1ea903617eee496d58d20aa
Neonatal Phototherapy Unit
FDA ID: b2d1f20bb1ea903617eee496d58d20aa
Device Classification
Brand Name
Bistos
Registration Information
Analysis ID
b2d1f20bb1ea903617eee496d58d20aa
Registration Date
September 28, 2022
Manufacturer
Name
Bistos Co., Ltd.Authorized Representative

