Taiwan FDA registration 8a555af01545a1eb711a3eb86b452502
"Kejie" precision adhesive (unsterilized)
TW: "可捷"精密接著體(未滅菌)
Taiwan·Risk Class 1·KJ MEDITECH CO., LTD.·Registered Sep 21, 2012 – Sep 21, 2017CancelledRegistration details
- Analysis ID
- 8a555af01545a1eb711a3eb86b452502
- Customs Code
- DHA04401219409
Company information
- Manufacturer
- KJ MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- New Tooth Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the "Precision Adhesive Body (F.3165)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3165 Precision Joints
- Import Information
- import
Dates and status
- Registration Date
- Sep 21, 2012
- Expiry Date
- Sep 21, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kejie" precision adhesive (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8a555af01545a1eb711a3eb86b452502 and manufactured by KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is New Tooth Technology Co., Ltd.
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