Taiwan FDA registration fb6e4af4dfc400d595191559b7d22687
"Kejie" dental hand instruments (unsterilized)
TW: “科潔”牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·KJ MEDITECH CO., LTD.·Registered Jul 31, 2009 – Jul 31, 2014CancelledRegistration details
- Analysis ID
- fb6e4af4dfc400d595191559b7d22687
- Customs Code
- DHA04400795001
Company information
- Manufacturer
- KJ MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- VISIONDENT COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
Dates and status
- Registration Date
- Jul 31, 2009
- Expiry Date
- Jul 31, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kejie" dental hand instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fb6e4af4dfc400d595191559b7d22687 and manufactured by KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is VISIONDENT COMPANY LIMITED.
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