ULTIMA R.P.R TEST KIT - FDA Registration 605cde558fbfbcbbac6e1c12d92a95f1
Access comprehensive regulatory information for ULTIMA R.P.R TEST KIT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 605cde558fbfbcbbac6e1c12d92a95f1 and manufactured by BEACON DIAGNOSTICS PVT. LTD. The device was registered on August 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
605cde558fbfbcbbac6e1c12d92a95f1
ULTIMA R.P.R TEST KIT
FDA ID: 605cde558fbfbcbbac6e1c12d92a95f1
Device Classification
Brand Name
BEACON
Registration Information
Analysis ID
605cde558fbfbcbbac6e1c12d92a95f1
Registration Date
August 18, 2022
Manufacturer
Authorized Representative

