Bond Enzyme Pretreatment Kit - FDA Registration a4c6466e88e1079a1451247fc5ad2079
Access comprehensive regulatory information for Bond Enzyme Pretreatment Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a4c6466e88e1079a1451247fc5ad2079 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
a4c6466e88e1079a1451247fc5ad2079
Bond Enzyme Pretreatment Kit
FDA ID: a4c6466e88e1079a1451247fc5ad2079
Device Classification
Brand Name
Leica
Registration Information
Analysis ID
a4c6466e88e1079a1451247fc5ad2079
Registration Date
December 15, 2021
Manufacturer
Authorized Representative

