Novocastra Reagents - FDA Registration e539dc8c25db30d37aec38de9308efc8
Access comprehensive regulatory information for Novocastra Reagents in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e539dc8c25db30d37aec38de9308efc8 and manufactured by Leica Biosystems Newcastle Ltd. The device was registered on January 18, 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
e539dc8c25db30d37aec38de9308efc8
Novocastra Reagents
FDA ID: e539dc8c25db30d37aec38de9308efc8
Device Classification
Brand Name
Leica
Registration Information
Analysis ID
e539dc8c25db30d37aec38de9308efc8
Registration Date
January 18, 2022
Manufacturer
Authorized Representative

