Taiwan FDA registration a2e193124d72183bf948107708883fc2
"Vertex" Endosseous dental implant accessories (Non-Sterile)
TW: "陀帝士" 牙齒骨內植入物附件 (未滅菌)
Taiwan·Risk Class 1·MD·VERTEX-DENTAL B.V.·Registered Mar 29, 2017 – Mar 29, 2027ActiveRegistration details
- Analysis ID
- a2e193124d72183bf948107708883fc2
- License Form
- Ministry of Health Medical Device Import No. 017662
- Customs Code
- DHA09401766208
Company information
- Manufacturer
- VERTEX-DENTAL B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- POPLAR CO., LTD.
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
- Mar 29, 2017
- Expiry Date
- Mar 29, 2027
About this record
Access comprehensive regulatory information for "Vertex" 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 a2e193124d72183bf948107708883fc2 and manufactured by VERTEX-DENTAL B.V.. The authorized representative in Taiwan is POPLAR 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.
Free DatabasePowered by Pure Global AI89,000+ Devices