Taiwan FDA registration c25c12e082bf411e4d64582b837f0937
“Teh Sen” External limb prosthetic component (Non-Sterile)
TW: “德森”體外肢體義肢用組件 (未滅菌)
Taiwan·Risk Class 1·MD·TEH SEN TECHNOLOGY INC.·Registered Oct 01, 2021 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- c25c12e082bf411e4d64582b837f0937
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 005443
Company information
- Manufacturer
- TEH SEN TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TEH SEN TECHNOLOGY INC.
Product details
- Intended Use
- Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3420 Components for in vitro limb prosthetics
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for “Teh Sen” External limb prosthetic component (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 c25c12e082bf411e4d64582b837f0937 and manufactured by TEH SEN TECHNOLOGY INC.. The authorized representative in Taiwan is TEH SEN TECHNOLOGY INC..
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