Myanmar FDA registration 49aed323822154a7142baf6e0b78db0f

Pericardial/Intracardiac Sumps

Myanmar·Medtronic·Viant Medical, Inc·Registered July 01, 2022

Device classification

Brand Name: Medtronic

Registration information

Analysis ID: 49aed323822154a7142baf6e0b78db0f
Registration Date: July 01, 2022

Manufacturer

Name: Viant Medical, Inc

Authorized Representative

Name: SEA LION COMPANY LIMITED

About this record

Access comprehensive regulatory information for Pericardial/Intracardiac Sumps in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 49aed323822154a7142baf6e0b78db0f and manufactured by Viant Medical, Inc. The device was registered on July 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.