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Myanmar FDA registration a2ab4c8838609d265645d3a18169c24f

DLP FLEXIBLE ARCH ARTERIAL CANNULA

Myanmar flagMyanmar·Medtronic·Viant Medical, Inc·Registered August 01, 2022
Device classification
Brand Name
Medtronic
Registration information
Analysis ID
a2ab4c8838609d265645d3a18169c24f
Registration Date
August 01, 2022
Manufacturer
Name
Viant Medical, Inc
Authorized Representative
Name
SEA LION COMPANY LIMITED
About this record

Access comprehensive regulatory information for DLP FLEXIBLE ARCH ARTERIAL CANNULA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a2ab4c8838609d265645d3a18169c24f and manufactured by Viant Medical, Inc. The device was registered on August 01, 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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