Pure Global

“Teh Sen” External limb prosthetic component (Non-Sterile) - Taiwan Registration c25c12e082bf411e4d64582b837f0937

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 Database
Powered by Pure Global AI
89,000+ Devices
c25c12e082bf411e4d64582b837f0937
Registration Details
Taiwan FDA Registration: c25c12e082bf411e4d64582b837f0937
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Teh Sen” External limb prosthetic component (Non-Sterile)
TW: “德森”體外肢體義肢用組件 (未滅菌)
Risk Class 1
MD

Registration Details

c25c12e082bf411e4d64582b837f0937

Ministry of Health Medical Device Manufacturing Registration No. 005443

Company Information

Taiwan, Province of China

Product Details

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.

o Equipment for physical medicine

O3420 Components for in vitro limb prosthetics

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2024