Taiwan FDA registration 77dfaa92fa67e18e72343e7a083c20af
“Bisco” All-Bond Universal Light-Cured Dental Adhesive
TW: “畢斯寇”歐棒光固化牙科黏著劑
Taiwan·Risk Class 2·MD·BISCO, INC.·Registered Jun 27, 2017 – Jun 27, 2027ActiveRegistration details
- Analysis ID
- 77dfaa92fa67e18e72343e7a083c20af
- License Form
- Ministry of Health Medical Device Import No. 029917
- Customs Code
- DHA05602991701
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)
- F3200 resin dental adhesive
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 27, 2017
- Expiry Date
- Jun 27, 2027
About this record
Access comprehensive regulatory information for “Bisco” All-Bond Universal Light-Cured Dental Adhesive in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77dfaa92fa67e18e72343e7a083c20af and manufactured by BISCO, INC.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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