Dengue NS1 Rapid Test Cassette ( Whole Blood / Serum / Plasma ) - FDA Registration 0b2811753ba5083be8f98c3d4df2c23f
Access comprehensive regulatory information for Dengue NS1 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 0b2811753ba5083be8f98c3d4df2c23f and manufactured by Qingdao Hightop Biotech Co.,Ltd. The device was registered on November 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.
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FDA Official Data
0b2811753ba5083be8f98c3d4df2c23f
Dengue NS1 Rapid Test Cassette ( Whole Blood / Serum / Plasma )
FDA ID: 0b2811753ba5083be8f98c3d4df2c23f
Device Classification
Brand Name
KANGHUA
Registration Information
Analysis ID
0b2811753ba5083be8f98c3d4df2c23f
Registration Date
November 10, 2022
Manufacturer
Authorized Representative

