Taiwan FDA registration 21952c39effeb5542bc36332473f7cbc
"Cole" Nether resin modified glass ion adhesive
TW: “科爾”奈瑟樹脂改良玻璃離子體黏合劑
Taiwan·Risk Class 2·KERR CORPORATION·Registered Jan 18, 2020 – Jan 18, 2030ActiveRegistration details
- Analysis ID
- 21952c39effeb5542bc36332473f7cbc
- Customs Code
- DHA05603316900
Company information
- Manufacturer
- KERR CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- NOBEL BIOCARE TAIWAN CO., LTD.
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.3275 牙科用水泥(士敏汀)
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2020
- Expiry Date
- Jan 18, 2030
About this record
Access comprehensive regulatory information for "Cole" Nether resin modified glass ion adhesive in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21952c39effeb5542bc36332473f7cbc and manufactured by KERR CORPORATION. The authorized representative in Taiwan is NOBEL BIOCARE TAIWAN 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