Taiwan FDA registration d96f5e1de595d45520a29728681e9b54
"Kejie" Duplu dental implant system
TW: “科潔”杜普露牙科植體系統
Taiwan·Risk Class 3·KJ MEDITECH CO., LTD.·Registered Apr 22, 2011 – Apr 22, 2026ExpiredRegistration details
- Analysis ID
- d96f5e1de595d45520a29728681e9b54
- Customs Code
- DHA00602234006
Company information
- Manufacturer
- KJ MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- VISIONDENT COMPANY LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3640 Bone Implants
- Import Information
- import
Dates and status
- Registration Date
- Apr 22, 2011
- Expiry Date
- Apr 22, 2026
About this record
Access comprehensive regulatory information for "Kejie" Duplu dental implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d96f5e1de595d45520a29728681e9b54 and manufactured by KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is VISIONDENT COMPANY LIMITED.
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