"Kinetec" Continuous Passive Motion Device (Non-sterile)
Taiwan·Risk Class 1·MD·KINETEC SAS·Registered Mar 15, 2018 – Mar 15, 2023Cancelled- Analysis ID
- dc322b2a5c2518814b411794a7c44539
- License Form
- Ministry of Health Medical Device Import No. 018898
- Customs Code
- DHA09401889803
- Manufacturer
- KINETEC SAS
- Manufacturer Country
- France
- Authorized Representative
- MAGISTRAL ENTERPRISE, INC.
- 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
- Mar 15, 2018
- Expiry Date
- Mar 15, 2023
- Cancellation Date
- May 19, 2021
- Status
- Logged out
- Reason
- 自請註銷
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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 dc322b2a5c2518814b411794a7c44539 and manufactured by KINETEC SAS. The authorized representative in Taiwan is MAGISTRAL ENTERPRISE, INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KINETEC, 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.