Taiwan FDA registration 585c0657dfc55f3871d47fbb5ce70857
Dai Swiss temporary smintin
TW: 戴瑞士臨時士敏汀
Registration details
- Analysis ID
- 585c0657dfc55f3871d47fbb5ce70857
- Customs Code
- DHA04400308707
Company information
- Manufacturer
- TEMREX CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- RECO-DENT INTERNATIONAL CO., LTD.
Product details
- Intended Use
- It is limited to the scope of the first level of identification of the medical device management measures (dental cement (Smintin) [F.3275]).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3275 牙科用水泥(士敏汀)
- Import Information
- import
Dates and status
- Registration Date
- Mar 23, 2006
- Expiry Date
- Mar 23, 2011
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Dai Swiss temporary smintin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 585c0657dfc55f3871d47fbb5ce70857 and manufactured by TEMREX CORPORATION. The authorized representative in Taiwan is RECO-DENT INTERNATIONAL 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