Taiwan FDA registration 3e6bb3110eac1675703f03c55e100131
"Kanit" continuous passive joint activator (unsterilized)
TW: "凱尼特" 連續式被動關節活動器(未滅菌)
Taiwan·Risk Class 1·KINETEC S.A.·Registered Mar 02, 2011 – Mar 02, 2016CancelledRegistration details
- Analysis ID
- 3e6bb3110eac1675703f03c55e100131
- Customs Code
- DHA04400997106
Company information
- Manufacturer
- KINETEC S.A.
- Manufacturer Country
- France
- Authorized Representative
- Jiatai Medical Equipment Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Continuous Passive Joint Activator (O.0006)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.0006 Continuous Passive Joint Movers
- Import Information
- import
Dates and status
- Registration Date
- Mar 02, 2011
- Expiry Date
- Mar 02, 2016
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kanit" continuous passive joint activator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3e6bb3110eac1675703f03c55e100131 and manufactured by KINETEC S.A.. The authorized representative in Taiwan is Jiatai Medical Equipment Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices