Taiwan FDA registration c0d7f3682d3c29b352f22a866ca7484b
"New Foden" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: “新福登”體外診斷用血庫離心機(未滅菌)
Taiwan·Risk Class 1·SILFRADENT SRL·Registered Jul 30, 2012 – Jul 30, 2017CancelledRegistration details
- Analysis ID
- c0d7f3682d3c29b352f22a866ca7484b
- Customs Code
- DHA04401199308
Company information
- Manufacturer
- SILFRADENT SRL
- Manufacturer Country
- Italy
- Authorized Representative
- DENTWEI INDUSTRY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 30, 2012
- Expiry Date
- Jul 30, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "New Foden" blood bank centrifuge for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0d7f3682d3c29b352f22a866ca7484b and manufactured by SILFRADENT SRL. The authorized representative in Taiwan is DENTWEI INDUSTRY CO., LTD..
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