Taiwan FDA registration 818db79baa2edcc4a95d32674d5254ca
"Chu Bai" Dentrong molded plastic dentures
TW: "楚拜" 登特容成形塑膠假牙
Taiwan·Risk Class 2·DENTSPLY TRUBYTE·Registered May 16, 2007 – May 16, 2022CancelledRegistration details
- Analysis ID
- 818db79baa2edcc4a95d32674d5254ca
- Customs Code
- DHA00601807501
Company information
- Manufacturer
- DENTSPLY TRUBYTE
- Manufacturer Country
- United States
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
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.3590 成型塑膠假牙床
- Import Information
- import
Dates and status
- Registration Date
- May 16, 2007
- Expiry Date
- May 16, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Chu Bai" Dentrong molded plastic dentures in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 818db79baa2edcc4a95d32674d5254ca and manufactured by DENTSPLY TRUBYTE. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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