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D-Dimmer Fast Test Kit ( Immunofluorescence Assay ) - FDA Registration 999b0a58474fcf338b05c9d1f3afbc1f

Access comprehensive regulatory information for D-Dimmer Fast Test Kit ( Immunofluorescence Assay ) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 999b0a58474fcf338b05c9d1f3afbc1f and manufactured by Getein Biotech , Inc. The device was registered on October 07, 2021.

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
999b0a58474fcf338b05c9d1f3afbc1f
D-Dimmer Fast Test Kit ( Immunofluorescence Assay )
FDA ID: 999b0a58474fcf338b05c9d1f3afbc1f
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Device Classification
Brand Name
Getein Biotech, Inc
Registration Information
Analysis ID
999b0a58474fcf338b05c9d1f3afbc1f
Registration Date
October 07, 2021
Manufacturer
Authorized Representative