H.Pylori Antibody Test Card - FDA Registration 6ae2c31c4edb90605f65c5f4030c70d8
Access comprehensive regulatory information for H.Pylori Antibody Test Card in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6ae2c31c4edb90605f65c5f4030c70d8 and manufactured by LumiQuick Diagnostics, Inc.. The device was registered on August 19, 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
6ae2c31c4edb90605f65c5f4030c70d8
H.Pylori Antibody Test Card
FDA ID: 6ae2c31c4edb90605f65c5f4030c70d8
Device Classification
Brand Name
Quick Profile
Registration Information
Analysis ID
6ae2c31c4edb90605f65c5f4030c70d8
Registration Date
August 19, 2022
Manufacturer
Authorized Representative

