Lactate Dehydrogenase (LDH) Kit (Rate Method) - FDA Registration a8fdaa31bfff8d387cf3d3424b2fd647
Access comprehensive regulatory information for Lactate Dehydrogenase (LDH) Kit (Rate Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a8fdaa31bfff8d387cf3d3424b2fd647 and manufactured by Zybio Inc.. The device was registered on December 16, 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
a8fdaa31bfff8d387cf3d3424b2fd647
Lactate Dehydrogenase (LDH) Kit (Rate Method)
FDA ID: a8fdaa31bfff8d387cf3d3424b2fd647
Device Classification
Brand Name
Zybio Inc.
Registration Information
Analysis ID
a8fdaa31bfff8d387cf3d3424b2fd647
Registration Date
December 16, 2022
Manufacturer
Name
Zybio Inc.Authorized Representative

