"Kinetec" continuous passive motion device (Non-sterile)
Taiwan·Risk Class 1·MD·KINETEC·Registered Jul 31, 2015 – Jul 31, 2020Cancelled- Analysis ID
- da8a71f0ced7c7934b649a3d61e3a70a
- License Form
- Ministry of Health Medical Device Import No. 015534
- Customs Code
- DHA09401553402
- Manufacturer
- KINETEC
- Manufacturer Country
- France
- Authorized Representative
- Lunxin Co., Ltd
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O0006 Continuous Passive Joint Activator
- Import Information
- Imported from abroad
- Registration Date
- Jul 31, 2015
- Expiry Date
- Jul 31, 2020
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Kinetec" continuous passive motion device (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 da8a71f0ced7c7934b649a3d61e3a70a and manufactured by KINETEC. The authorized representative in Taiwan is Lunxin Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KINETEC SAS, 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.