Myanmar FDA registration cd9bd603004adc1a1b5bf6567cfd1b1f
Anti-Fluorescein Antibody
Device classification
- Brand Name
- Leica
Registration information
- Analysis ID
- cd9bd603004adc1a1b5bf6567cfd1b1f
- Registration Date
- December 15, 2021
Manufacturer
Authorized Representative
About this record
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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