Taiwan FDA registration 2ef82b4d389933a7733f56e3774cff32
"Jiastar" CAD/CAM optical mold taking system (unsterilized)
TW: “佳世達” CAD/CAM光學取模系統 (未滅菌)
Taiwan·Risk Class 1·Jiastar Technology Co., Ltd. Double Star Factory 2·Registered Aug 10, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 2ef82b4d389933a7733f56e3774cff32
- Customs Code
- DHA083a0026502
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- QISDA CORPORATION
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
- Import Information
- Medical equipment manufactured in bonded factories
Dates and status
- Registration Date
- Aug 10, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Jiastar" CAD/CAM optical mold taking 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 2ef82b4d389933a7733f56e3774cff32 and manufactured by Jiastar Technology Co., Ltd. Double Star Factory 2. The authorized representative in Taiwan is QISDA CORPORATION.
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