Taiwan FDA registration eef68c220e1612580d4d9ecd12d2b842
“B&E” Light-cured Composite Resin
TW: “賓益”樹脂牙材
Taiwan·Risk Class 2·MD·B&E KOREA CO., LTD·Registered Jul 31, 2021 – Jul 31, 2026ActiveRegistration details
- Analysis ID
- eef68c220e1612580d4d9ecd12d2b842
- License Form
- Ministry of Health Medical Device Import No. 034798
- Customs Code
- DHA05603479800
Company information
- Manufacturer
- B&E KOREA CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- YOUNG SUN DEVELOP CO.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Jul 31, 2021
- Expiry Date
- Jul 31, 2026
About this record
Access comprehensive regulatory information for “B&E” Light-cured Composite Resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eef68c220e1612580d4d9ecd12d2b842 and manufactured by B&E KOREA CO., LTD. The authorized representative in Taiwan is YOUNG SUN DEVELOP CO..
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