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Syphilis Rapid Test Dipstick (Whole Blood/ Serum/ Plasma) - FDA Registration c4e269ca8909abbf92fe56040f5c87ae

Access comprehensive regulatory information for Syphilis Rapid Test Dipstick (Whole Blood/ Serum/ Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c4e269ca8909abbf92fe56040f5c87ae and manufactured by ACRO BIOTECH INC.. The device was registered on August 24, 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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c4e269ca8909abbf92fe56040f5c87ae
Syphilis Rapid Test Dipstick (Whole Blood/ Serum/ Plasma)
FDA ID: c4e269ca8909abbf92fe56040f5c87ae
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Device Classification
Brand Name
TVI
Registration Information
Analysis ID
c4e269ca8909abbf92fe56040f5c87ae
Registration Date
August 24, 2022
Manufacturer
Authorized Representative