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“Uniprox”External limb prosthetic component (Non-Sterile) - Taiwan Registration 6a3317cbb2fd2bb698145b144c269820

Access comprehensive regulatory information for “Uniprox”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 6a3317cbb2fd2bb698145b144c269820 and manufactured by Uniprox GmbH & Co. KG. The authorized representative in Taiwan is TEH LIN PROSTHETIC & ORTHOPAEDIC INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Uniprox GmbH & Co. KG, and 1 recent registrations in the same category. 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.

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6a3317cbb2fd2bb698145b144c269820
Registration Details
Taiwan FDA Registration: 6a3317cbb2fd2bb698145b144c269820
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Device Details

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

Registration Details

6a3317cbb2fd2bb698145b144c269820

Ministry of Health Medical Device Import Registration No. 022100

DHA08402210003

Company Information

Germany

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

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

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