“PROTEOR” External Limb Prosthetic Component (Non-Sterile)
Taiwan·Risk Class 1·MD·PROTEOR USA·Registered Mar 17, 2021 – Mar 17, 2026Cancelled- Analysis ID
- dfbc36f7b58728a745ddfa1347fa4f1a
- License Form
- Ministry of Health Medical Device Import No. 022393
- Customs Code
- DHA09402239301
- Manufacturer
- PROTEOR USA
- Manufacturer Country
- United States
- Authorized Representative
- KEN DALL ENTERPRISE CO., LTD.
- 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
- Mar 17, 2021
- Expiry Date
- Mar 17, 2026
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for “PROTEOR” 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 dfbc36f7b58728a745ddfa1347fa4f1a and manufactured by PROTEOR USA. 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 PROTEOR USA, 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.