Taiwan FDA registration 5feb078fb58f40f260a994fb3bc06e09
Kiki dental root canal file (unsterilized)
TW: "奇祁"牙科根管銼 (未滅菌)
Taiwan·Risk Class 1·INNOVATIVE MATERIAL AND DEVICES, INC·Registered Dec 03, 2015 – Dec 03, 2025ExpiredRegistration details
- Analysis ID
- 5feb078fb58f40f260a994fb3bc06e09
- Customs Code
- DHA09600258300
Company information
- Manufacturer
- INNOVATIVE MATERIAL AND DEVICES, INC
- Manufacturer Country
- China
- Authorized Representative
- DHEF INC.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of 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
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 03, 2015
- Expiry Date
- Dec 03, 2025
About this record
Access comprehensive regulatory information for Kiki dental root canal file (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5feb078fb58f40f260a994fb3bc06e09 and manufactured by INNOVATIVE MATERIAL AND DEVICES, INC. The authorized representative in Taiwan is DHEF INC..
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