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Myanmar FDA registration 56106681ab297152d7ef44582ee41caf

Dengue Ag and Ab Combo Rapid Test Cassette (Whole Blood/ Serum/ Plasma)

MyanmarRightSignHangzhou Biotest Biotech Co., Ltd.Registered July 01, 2022
VerifiedFDA Myanmar · official registry
Device classification
Brand Name
RightSign
Registration information
Analysis ID
56106681ab297152d7ef44582ee41caf
Registration Date
July 01, 2022
Manufacturer
Name
Hangzhou Biotest Biotech Co., Ltd.
Authorized Representative
Name
FOCUS HEALTH COMPANY LIMITED
About this record

Access comprehensive regulatory information for Dengue Ag and Ab Combo Rapid Test Cassette (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 56106681ab297152d7ef44582ee41caf and manufactured by Hangzhou Biotest Biotech Co., Ltd.. The device was registered on July 01, 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.