“Fillauer” External Limb Prosthetic Component (Non-Sterile)
Taiwan·Risk Class 1·MD·FILLAUER LLC·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 6342a35c8e017ae97615baee5750f500
- License Form
- Ministry of Health Medical Device Import Registration No. 022392
- Customs Code
- DHA08402239203
- Manufacturer
- FILLAUER LLC
- Manufacturer Country
- United States
- Authorized Representative
- KEN DALL ENTERPRISE CO., LTD.
- 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
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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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.