Taiwan FDA registration f5153a57e91f7d5101b59bdf93eb7fa4
“Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Liner
TW: “畢斯寇”光固化矽酸鈣襯底材
Taiwan·Risk Class 2·MD·BISCO, INC.·Registered Sep 28, 2018 – Sep 28, 2028ActiveRegistration details
- Analysis ID
- f5153a57e91f7d5101b59bdf93eb7fa4
- License Form
- Ministry of Health Medical Device Import No. 031646
- Customs Code
- DHA05603164601
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)
- F3250 Calcium hydroxide cavity substrate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 28, 2018
- Expiry Date
- Sep 28, 2028
About this record
Access comprehensive regulatory information for “Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Liner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5153a57e91f7d5101b59bdf93eb7fa4 and manufactured by BISCO, INC.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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