Taiwan FDA registration be9e09c6988516b3f480f599ac566cc5
"CORE3D" Endosseous dental implant accessories (non-sterile)
TW: "克爾三迪" 牙齒骨內植入物附件 (未滅菌)
Registration details
- Analysis ID
- be9e09c6988516b3f480f599ac566cc5
- License Form
- Ministry of Health Medical Device Import No. 017314
- Customs Code
- DHA09401731401
Company information
- Manufacturer
- AVINENT IMPLANT SYSTEM S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 20, 2016
- Expiry Date
- Dec 20, 2021
About this record
Access comprehensive regulatory information for "CORE3D" Endosseous dental implant accessories (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 be9e09c6988516b3f480f599ac566cc5 and manufactured by AVINENT IMPLANT SYSTEM S.L.. The authorized representative in Taiwan is HI-CLEARANCE INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices