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Bioline H.pylori Ag - FDA Registration 72ed2abbde8817393e4397e5c0ec0ed0

Access comprehensive regulatory information for Bioline H.pylori Ag in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 72ed2abbde8817393e4397e5c0ec0ed0 and manufactured by Abbott Diagnostics Korea Inc.. The device was registered on March 25, 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
72ed2abbde8817393e4397e5c0ec0ed0
Bioline H.pylori Ag
FDA ID: 72ed2abbde8817393e4397e5c0ec0ed0
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DJ Fang

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Device Classification
Brand Name
Bioline
Registration Information
Analysis ID
72ed2abbde8817393e4397e5c0ec0ed0
Registration Date
March 25, 2022
Authorized Representative