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“Fillauer” External Limb Prosthetic Component (Non-Sterile) - Taiwan Registration 6342a35c8e017ae97615baee5750f500

Access comprehensive regulatory information for “Fillauer” 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 6342a35c8e017ae97615baee5750f500 and manufactured by FILLAUER LLC. The authorized representative in Taiwan is KEN DALL ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FILLAUER LLC, 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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6342a35c8e017ae97615baee5750f500
Registration Details
Taiwan FDA Registration: 6342a35c8e017ae97615baee5750f500
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Device Details

“Fillauer” External Limb Prosthetic Component (Non-Sterile)
TW: “費老兒” 體外肢體義肢用組件(未滅菌)
Risk Class 1
MD

Registration Details

6342a35c8e017ae97615baee5750f500

Ministry of Health Medical Device Import Registration No. 022392

DHA08402239203

Company Information

United States

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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