Taiwan FDA registration 00692fbce85a2750287681db54a0ac67
“Bisco” CORE-FLO DC Lite Dual-Cured Low Viscosity Core Build-up Material
TW: “畢斯寇”雙向固化冠心複合樹脂
Taiwan·Risk Class 2·MD·BISCO, INC.·Registered Jun 22, 2018 – Jun 22, 2028ActiveRegistration details
- Analysis ID
- 00692fbce85a2750287681db54a0ac67
- License Form
- Ministry of Health Medical Device Import No. 031258
- Customs Code
- DHA05603125802
Company information
- Manufacturer
- BISCO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 22, 2018
- Expiry Date
- Jun 22, 2028
About this record
Access comprehensive regulatory information for “Bisco” CORE-FLO DC Lite Dual-Cured Low Viscosity Core Build-up Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 00692fbce85a2750287681db54a0ac67 and manufactured by BISCO, INC.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL 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