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HIV 1.2 Rapid Test Dipstick (Whole Blood/Serum/Plasma) - FDA Registration f6ec5c6e8db0a6d04c8acf6b22e68786

Access comprehensive regulatory information for HIV 1.2 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 f6ec5c6e8db0a6d04c8acf6b22e68786 and manufactured by ACRO BIOTECH INC.. The device was registered on October 19, 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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f6ec5c6e8db0a6d04c8acf6b22e68786
HIV 1.2 Rapid Test Dipstick (Whole Blood/Serum/Plasma)
FDA ID: f6ec5c6e8db0a6d04c8acf6b22e68786
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Device Classification
Brand Name
TVI
Registration Information
Analysis ID
f6ec5c6e8db0a6d04c8acf6b22e68786
Registration Date
October 19, 2022
Manufacturer
Authorized Representative