Taiwan FDA registration 2410a5fb11540985d05a442a8a83986c
“Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Protectant/Liner
TW: “畢氏”光固化矽酸鈣襯底材
Taiwan·Risk Class 2·MD·BISCO, INC.·Registered Jul 15, 2014 – Jul 15, 2024ExpiredRegistration details
- Analysis ID
- 2410a5fb11540985d05a442a8a83986c
- License Form
- Ministry of Health Medical Device Import No. 026342
- Customs Code
- DHA05602634200
Company information
- Manufacturer
- BISCO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- KUO HWA DENTAL SUPPLIERS CO., LTD.
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)
- F3250 Calcium hydroxide cavity substrate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 15, 2014
- Expiry Date
- Jul 15, 2024
About this record
Access comprehensive regulatory information for “Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Protectant/Liner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2410a5fb11540985d05a442a8a83986c and manufactured by BISCO, INC.. The authorized representative in Taiwan is KUO HWA DENTAL SUPPLIERS CO., LTD..
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