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One Step H. pylori Ag Rapid Test Cassette (Feces) - FDA Registration 0ad64323e48c3a5f450e5dda9ba63631

Access comprehensive regulatory information for One Step H. pylori Ag Rapid Test Cassette (Feces) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0ad64323e48c3a5f450e5dda9ba63631 and manufactured by Nantong Diagnos Biotechnology Co., Ltd. The device was registered on November 15, 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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0ad64323e48c3a5f450e5dda9ba63631
One Step H. pylori Ag Rapid Test Cassette (Feces)
FDA ID: 0ad64323e48c3a5f450e5dda9ba63631
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Device Classification
Brand Name
DIAGNOSIS
Registration Information
Analysis ID
0ad64323e48c3a5f450e5dda9ba63631
Registration Date
November 15, 2022
Authorized Representative