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ichroma AMH - FDA Registration dc402018ec39cea273d26ea0def492be

Access comprehensive regulatory information for ichroma AMH in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dc402018ec39cea273d26ea0def492be and manufactured by Boditech Med Inc.. The device was registered on November 30, 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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dc402018ec39cea273d26ea0def492be
ichroma AMH
FDA ID: dc402018ec39cea273d26ea0def492be
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Device Classification
Brand Name
ichroma
Registration Information
Analysis ID
dc402018ec39cea273d26ea0def492be
Registration Date
November 30, 2022