Taiwan FDA registration 553b0e1fd59dbc8173b5b730eb64bb1b
"Kubota" Blood bag refrigeration eccentricity machine (unsterilized)
TW: "久保田" 血袋用冷凍離心機 (未滅菌)
Taiwan·Risk Class 1·KUBOTA MFG. CORP. FUJIOKA PLANT·Registered Sep 16, 2008 – Sep 16, 2018CancelledRegistration details
- Analysis ID
- 553b0e1fd59dbc8173b5b730eb64bb1b
- Customs Code
- DHA04400707102
Company information
- Manufacturer
- KUBOTA MFG. CORP. FUJIOKA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- DOUBLE EAGLE ENTERPRISE 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
- import
Dates and status
- Registration Date
- Sep 16, 2008
- Expiry Date
- Sep 16, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kubota" Blood bag refrigeration eccentricity machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 553b0e1fd59dbc8173b5b730eb64bb1b and manufactured by KUBOTA MFG. CORP. FUJIOKA PLANT. The authorized representative in Taiwan is DOUBLE EAGLE ENTERPRISE CO., LTD..
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