Taiwan FDA registration a8a8e823b748ae22106d5b0835b2033d
“Bicon” Abutment
TW: “拜肯”牙科用植體基柱
Taiwan·Risk Class 2·MD·Bicon, LLC·Registered Aug 11, 2023 – Aug 11, 2028ActiveRegistration details
- Analysis ID
- a8a8e823b748ae22106d5b0835b2033d
- License Form
- Ministry of Health Medical Device Import No. 036692
- Customs Code
- DHA05603669204
Company information
- Manufacturer
- Bicon, LLC
- Manufacturer Country
- United States
- Authorized Representative
- BICON TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F3630 Bone explant supports
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 11, 2023
- Expiry Date
- Aug 11, 2028
About this record
Access comprehensive regulatory information for “Bicon” Abutment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a8a8e823b748ae22106d5b0835b2033d and manufactured by Bicon, LLC. The authorized representative in Taiwan is BICON TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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