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“Fillauer” External Limb Prosthetic Component (Non-Sterile) - Taiwan Registration 38672a2a86b70aedae5e23a938e6ac87

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 38672a2a86b70aedae5e23a938e6ac87 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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38672a2a86b70aedae5e23a938e6ac87
Registration Details
Taiwan FDA Registration: 38672a2a86b70aedae5e23a938e6ac87
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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
Cancelled

Registration Details

38672a2a86b70aedae5e23a938e6ac87

Ministry of Health Medical Device Import No. 022392

DHA09402239202

Company Information

United States

Product Details

o Equipment for physical medicine

O3420 Components for in vitro limb prosthetics

Imported from abroad

Dates and Status

Mar 17, 2021

Mar 17, 2026

Cancellation Information

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