Taiwan FDA registration 6a3317cbb2fd2bb698145b144c269820

“Uniprox”External limb prosthetic component (Non-Sterile)

TW: “優派”體外肢體義肢用組件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Uniprox GmbH & Co. KG·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
6a3317cbb2fd2bb698145b144c269820
License Form
Ministry of Health Medical Device Import Registration No. 022100
Customs Code
DHA08402210003
Company information
Manufacturer Country
Germany
Authorized Representative
TEH LIN PROSTHETIC & ORTHOPAEDIC 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
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

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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