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MaxLINE Syphilis/TP Rapid Test - FDA Registration 066ffc52a848dff7f39a14a74a72c3c4

Access comprehensive regulatory information for MaxLINE Syphilis/TP Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 066ffc52a848dff7f39a14a74a72c3c4 and manufactured by Avecon Healthcare Pvt. Ltd.. The device was registered on July 27, 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
066ffc52a848dff7f39a14a74a72c3c4
MaxLINE Syphilis/TP Rapid Test
FDA ID: 066ffc52a848dff7f39a14a74a72c3c4
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Device Classification
Brand Name
MaxLINE
Registration Information
Analysis ID
066ffc52a848dff7f39a14a74a72c3c4
Registration Date
July 27, 2022