Taiwan FDA registration 2ab3af58204b714209cf7dce39d634be
“B&E”Base Plate Shellac (Non-Sterile)
TW: “比隱依”基底塗料 (未滅菌)
Taiwan·Risk Class 1·MD·B&E KOREA CO., LTD·Registered Jun 11, 2020 – Jun 11, 2025ExpiredRegistration details
- Analysis ID
- 2ab3af58204b714209cf7dce39d634be
- License Form
- Ministry of Health Medical Device Import No. 021627
- Customs Code
- DHA09402162708
Company information
- Manufacturer
- B&E KOREA CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Mi Luo International Limited Company
Product details
- Intended Use
- Limited to the first level identification range of base coatings (F.6200) of the medical equipment management measures.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6200 base coating
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 11, 2020
- Expiry Date
- Jun 11, 2025
About this record
Access comprehensive regulatory information for “B&E”Base Plate Shellac (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2ab3af58204b714209cf7dce39d634be and manufactured by B&E KOREA CO., LTD. The authorized representative in Taiwan is Mi Luo International Limited Company.
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