Dade Actin FSL Activated PTT Reagent - FDA Registration adf0ed0b1f8081c9c6eebf0fb241c2ba
Access comprehensive regulatory information for Dade Actin FSL Activated PTT Reagent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID adf0ed0b1f8081c9c6eebf0fb241c2ba and manufactured by Siemens Healthcare Diagnostics Products GmbH. The device was registered on February 08, 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
adf0ed0b1f8081c9c6eebf0fb241c2ba
Dade Actin FSL Activated PTT Reagent
FDA ID: adf0ed0b1f8081c9c6eebf0fb241c2ba
Device Classification
Brand Name
Siemens
Registration Information
Analysis ID
adf0ed0b1f8081c9c6eebf0fb241c2ba
Registration Date
February 08, 2022
Manufacturer
Authorized Representative

