Defibrillation System - TEC-5631K - FDA Registration be4fa8978dbf15371c15594099c107f4

Access comprehensive regulatory information for Defibrillation System - TEC-5631K in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID be4fa8978dbf15371c15594099c107f4 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on June 02, 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.