Taiwan FDA registration c360f19f7f6fb6e3fa2c48ce69e41e09
Taiwan Ruili CAD/CAM Optical Mold System (Unsterilized)
TW: 台灣瑞麗 CAD/CAM光學取模系統 (未滅菌)
Taiwan·Risk Class 1·DDS Inc.·Registered Feb 16, 2022 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- c360f19f7f6fb6e3fa2c48ce69e41e09
- Customs Code
- DHA084a0008900
Company information
- Manufacturer
- DDS Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Rayscan Taiwan CO., Ltd
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
- Feb 16, 2022
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Taiwan Ruili CAD/CAM Optical Mold 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 c360f19f7f6fb6e3fa2c48ce69e41e09 and manufactured by DDS Inc.. The authorized representative in Taiwan is Rayscan 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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