Taiwan FDA registration 84bae6d0222b756fd6e032b1c1b09b6f

"TANAX" SUPPORTER (Non-Sterile)

TW: "鈦奈克斯" 醫療用護具(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TANAX CO., LTD·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
84bae6d0222b756fd6e032b1c1b09b6f
License Form
Ministry of Health Medical Device Import Registration No. 010641
Customs Code
DHA08401064108
Company information
Manufacturer
TANAX CO., LTD
Manufacturer Country
Japan
Authorized Representative
SUN MANAGEMENT CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3475 Body Equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
About this record

Access comprehensive regulatory information for "TANAX" SUPPORTER (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 84bae6d0222b756fd6e032b1c1b09b6f and manufactured by TANAX CO., LTD. The authorized representative in Taiwan is SUN MANAGEMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices