Taiwan FDA registration ada55293061bf511880464c240d611ab
Centrifugal biochemical analyzer for clinical use of "New Foden" (unsterilized)
TW: “新福登”臨床使用的離心式生化分析儀 (未滅菌)
Taiwan·Risk Class 1·SILFRADENT S.R.L.·Registered Jul 17, 2017 – Jul 17, 2022CancelledRegistration details
- Analysis ID
- ada55293061bf511880464c240d611ab
- Customs Code
- DHA09401807001
Company information
- Manufacturer
- SILFRADENT S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DENTWEI INDUSTRY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "centrifugal biochemical analyzer for clinical use (A.2140)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2140 Centrifugal biochemistry analyzer for clinical use
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 17, 2017
- Expiry Date
- Jul 17, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Centrifugal biochemical analyzer for clinical use of "New Foden" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ada55293061bf511880464c240d611ab and manufactured by SILFRADENT S.R.L.. The authorized representative in Taiwan is DENTWEI INDUSTRY CO., LTD..
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