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Myanmar FDA registration be4fa8978dbf15371c15594099c107f4

Defibrillation System - TEC-5631K

MyanmarTowards NihoNihon Kohden Tomioka Corporation Tomioka Production CenterRegistered June 02, 2022
VerifiedFDA Myanmar · official registry
Device classification
Brand Name
Towards Niho
Registration information
Analysis ID
be4fa8978dbf15371c15594099c107f4
Registration Date
June 02, 2022
Manufacturer
Name
Nihon Kohden Tomioka Corporation Tomioka Production Center
Authorized Representative
Name
YEE SHIN COMPANY LIMITED
About this record

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.