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ichroma CEA Neo - FDA Registration 7ba8727fa48b602ff8e6d133ee6f2892

Access comprehensive regulatory information for ichroma CEA Neo in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7ba8727fa48b602ff8e6d133ee6f2892 and manufactured by Boditech Med Inc.. The device was registered on November 04, 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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7ba8727fa48b602ff8e6d133ee6f2892
ichroma CEA Neo
FDA ID: 7ba8727fa48b602ff8e6d133ee6f2892
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Device Classification
Brand Name
ichroma
Registration Information
Analysis ID
7ba8727fa48b602ff8e6d133ee6f2892
Registration Date
November 04, 2022