ONE STEP Anti-HIV (1&2) Tri-line Test (Whole Blood/Serum/Plasma) - FDA Registration 6ed628113c74ecbc908ec686498fbbda
Access comprehensive regulatory information for ONE STEP Anti-HIV (1&2) Tri-line Test (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 6ed628113c74ecbc908ec686498fbbda and manufactured by InTec PRODUCTS, INC.. The device was registered on October 30, 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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6ed628113c74ecbc908ec686498fbbda
ONE STEP Anti-HIV (1&2) Tri-line Test (Whole Blood/Serum/Plasma)
FDA ID: 6ed628113c74ecbc908ec686498fbbda
Device Classification
Brand Name
ADVANCED QUALITY
Registration Information
Analysis ID
6ed628113c74ecbc908ec686498fbbda
Registration Date
October 30, 2022
Manufacturer
Authorized Representative

