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Myanmar FDA registration 0524becf7db6d00a04a233d84542e11b

Sleep Diagnostic System

MyanmarTowards NihoNihon Kohden Tomioka Corporation Tomioka Production CenterRegistered July 14, 2022
VerifiedFDA Myanmar · official registry
Device classification
Brand Name
Towards Niho
Registration information
Analysis ID
0524becf7db6d00a04a233d84542e11b
Registration Date
July 14, 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 Sleep Diagnostic System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0524becf7db6d00a04a233d84542e11b and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on July 14, 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.