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Anti-Fluorescein Antibody - FDA Registration cd9bd603004adc1a1b5bf6567cfd1b1f

Access comprehensive regulatory information for Anti-Fluorescein Antibody in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cd9bd603004adc1a1b5bf6567cfd1b1f and manufactured by Leica Biosystems Newcastle Ltd. The device was registered on December 15, 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
cd9bd603004adc1a1b5bf6567cfd1b1f
Anti-Fluorescein Antibody
FDA ID: cd9bd603004adc1a1b5bf6567cfd1b1f
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Device Classification
Brand Name
Leica
Registration Information
Analysis ID
cd9bd603004adc1a1b5bf6567cfd1b1f
Registration Date
December 15, 2021