Taiwan FDA registration 7d388ea077932db97ce35b0e6a501e4e
“KJ” Narrow Body Screw System
TW: “可捷”窄體人工牙根
Taiwan·Risk Class 3·MD·KJ MEDITECH CO., LTD.·Registered Nov 21, 2011 – Nov 21, 2026ActiveRegistration details
- Analysis ID
- 7d388ea077932db97ce35b0e6a501e4e
- License Form
- Department of Health Medical Device Import No. 023017
- Customs Code
- DHA00602301704
Company information
- Manufacturer
- KJ MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Jinpin Technology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3640 Bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 21, 2011
- Expiry Date
- Nov 21, 2026
About this record
Access comprehensive regulatory information for “KJ” Narrow Body Screw System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7d388ea077932db97ce35b0e6a501e4e and manufactured by KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is Jinpin Technology Co., Ltd.
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