Malaria P.f./P.v. Rapid Test Cassette (Whole Blood) - FDA Registration 007f22b9bf35dbb49daa2e156ac01b26
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 007f22b9bf35dbb49daa2e156ac01b26 and manufactured by Hangzhou AllTest Biotech Co., Ltd.. The device was registered on May 10, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
007f22b9bf35dbb49daa2e156ac01b26
Malaria P.f./P.v. Rapid Test Cassette (Whole Blood)
FDA ID: 007f22b9bf35dbb49daa2e156ac01b26
Device Classification
Brand Name
ALLTEST
Registration Information
Analysis ID
007f22b9bf35dbb49daa2e156ac01b26
Registration Date
May 10, 2022
Manufacturer
Authorized Representative

