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Myanmar FDA registration f576be75498d385c2a340be2934b8210

DLP Straight Tip Arterial Cannula

Myanmar flagMyanmar·Medtronic·Viant Medical, Inc·Registered August 08, 2022
Device classification
Brand Name
Medtronic
Registration information
Analysis ID
f576be75498d385c2a340be2934b8210
Registration Date
August 08, 2022
Manufacturer
Name
Viant Medical, Inc
Authorized Representative
Name
SEA LION COMPANY LIMITED
About this record

Access comprehensive regulatory information for DLP Straight Tip Arterial Cannula in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f576be75498d385c2a340be2934b8210 and manufactured by Viant Medical, Inc. The device was registered on August 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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