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ichroma™ COVID-19 From - FDA Registration 329773a8b5fc0b253a0a1a9fb729fa25

Access comprehensive regulatory information for ichroma™ COVID-19 From in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 329773a8b5fc0b253a0a1a9fb729fa25 and manufactured by Boditech Med Inc. The device was registered on October 15, 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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FDA Official Data
329773a8b5fc0b253a0a1a9fb729fa25
ichroma™ COVID-19 From
FDA ID: 329773a8b5fc0b253a0a1a9fb729fa25
Local name: ichroma™ COVID-19 Ab
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Device Classification
Brand Name
Boditech
Registration Information
Analysis ID
329773a8b5fc0b253a0a1a9fb729fa25
Registration Date
October 15, 2021
Manufacturer
Authorized Representative