"Streifeneder" External limb prosthetic component (Non-Sterile)
Taiwan·Risk Class 1·MD·STREIFENEDER ORTHO. PRODUCTION GMBH·Registered Dec 27, 2018 – Dec 27, 2023Cancelled- Analysis ID
- b5ef0c5f60114129c291b913ace77168
- License Form
- Ministry of Health Medical Device Import No. 019968
- Customs Code
- DHA09401996803
- Manufacturer
- STREIFENEDER ORTHO. PRODUCTION GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- JEN DER P&O APPLIANCES MANUFACTURING 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
- Dec 27, 2018
- Expiry Date
- Dec 27, 2023
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Streifeneder" 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 b5ef0c5f60114129c291b913ace77168 and manufactured by STREIFENEDER ORTHO. PRODUCTION GMBH. The authorized representative in Taiwan is JEN DER P&O APPLIANCES MANUFACTURING CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STREIFENEDER ORTHO. PRODUCTION GMBH, and 2 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.