Malaria P.f./ P.v. Rapid Test Cassette (Whole Blood) - FDA Registration 56c8dd8c932a28fd2cca0710c2e70ba4
Access comprehensive regulatory information for Malaria P.f./ P.v. Rapid Test Cassette (Whole Blood) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 56c8dd8c932a28fd2cca0710c2e70ba4 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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56c8dd8c932a28fd2cca0710c2e70ba4
Malaria P.f./ P.v. Rapid Test Cassette (Whole Blood)
FDA ID: 56c8dd8c932a28fd2cca0710c2e70ba4
Device Classification
Brand Name
TVI
Registration Information
Analysis ID
56c8dd8c932a28fd2cca0710c2e70ba4
Registration Date
August 24, 2022
Manufacturer
Authorized Representative

