Taiwan FDA registration 516f162fbb38f7e4e6d17a5a9327b105
Kubota Blood Chamber Eccentricity (Unsterilized)
TW: 久保田 體外診斷用血庫離心機 (未滅菌)
Taiwan·Risk Class 1·KUBOTA MFG. CORP. FUJIOKA PLANT·Registered Oct 05, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 516f162fbb38f7e4e6d17a5a9327b105
- Customs Code
- DHA084a0022801
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 classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
Dates and status
- Registration Date
- Oct 05, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Kubota Blood Chamber Eccentricity (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 516f162fbb38f7e4e6d17a5a9327b105 and manufactured by KUBOTA MFG. CORP. FUJIOKA PLANT. The authorized representative in Taiwan is DOUBLE EAGLE ENTERPRISE CO., LTD..
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