Taiwan FDA registration d3f06e4f628c23d34d6d4e4b7a4198ba
"Ivoca Vadent" CAD/CAM Optical Moulding System (Unsterilized)
TW: “義獲嘉偉瓦登特” CAD/CAM光學取模系統 (未滅菌)
Taiwan·Risk Class 1·Ivoclar Vivadent Manufacturing GmbH;;IVOCLAR VIVADENT AG·Registered May 03, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- d3f06e4f628c23d34d6d4e4b7a4198ba
- Customs Code
- DHA084a0017404
Company information
- Manufacturer Country
- Austria;;Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, CAD/CAM optical mold taking system (F.3661) first level recognition range.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3661 CAD/CAM光學取模系統
Dates and status
- Registration Date
- May 03, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Ivoca Vadent" CAD/CAM Optical Moulding System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d3f06e4f628c23d34d6d4e4b7a4198ba and manufactured by Ivoclar Vivadent Manufacturing GmbH;;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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