Taiwan FDA registration 64f600f9fd897b474cca24219547fda9
"Ke Ting" sea root canal needle (sterilization)
TW: “柯汀” 海芙根管銼針 (滅菌)
Taiwan·Risk Class 1·COLTENE/WHALEDENT GMBH+CO. KG·Registered Jul 24, 2020 – Jul 24, 2025ExpiredRegistration details
- Analysis ID
- 64f600f9fd897b474cca24219547fda9
- Customs Code
- DHA09402178105
Company information
- Manufacturer
- COLTENE/WHALEDENT GMBH+CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- LEADING WAVE RA CO., LTD.
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;; QMS/QSD
Dates and status
- Registration Date
- Jul 24, 2020
- Expiry Date
- Jul 24, 2025
About this record
Access comprehensive regulatory information for "Ke Ting" sea root canal needle (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 64f600f9fd897b474cca24219547fda9 and manufactured by COLTENE/WHALEDENT GMBH+CO. KG. The authorized representative in Taiwan is LEADING WAVE RA CO., LTD..
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