Defibrillation System - TEC-5621K and TEC-5631K - FDA Registration f6b7db5b3f45fa7c6f171cf1117486af

Access comprehensive regulatory information for Defibrillation System - TEC-5621K and TEC-5631K in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f6b7db5b3f45fa7c6f171cf1117486af and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on May 17, 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.