Myanmar FDA registration 3cf1d89e49edf0e9d77fdaf21e2286f0

DLP Pulmonary Artery Vent Cannula

Myanmar·Medtronic·Viant Medical, Inc·Registered July 20, 2022

Device classification

Brand Name: Medtronic

Registration information

Analysis ID: 3cf1d89e49edf0e9d77fdaf21e2286f0
Registration Date: July 20, 2022

Manufacturer

Name: Viant Medical, Inc

Authorized Representative

Name: SEA LION COMPANY LIMITED

About this record

Access comprehensive regulatory information for DLP Pulmonary Artery Vent Cannula in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3cf1d89e49edf0e9d77fdaf21e2286f0 and manufactured by Viant Medical, Inc. The device was registered on July 20, 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.