Taiwan FDA registration 63f850e611d454ec1831a85c6dcf62ca
Kubota blood cell volume measurement device (unsterilized)
TW: "久保田"血球容積測量裝置(未滅菌)
Taiwan·Risk Class 1·KUBOTA MFG. CORP. FUJIOKA PLANT·Registered Oct 24, 2013 – Oct 24, 2023ExpiredRegistration details
- Analysis ID
- 63f850e611d454ec1831a85c6dcf62ca
- Customs Code
- DHA09401353201
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 the "Blood Cell Volume Measuring Device (B.6400)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.6400 Hemocytometry device
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Oct 24, 2013
- Expiry Date
- Oct 24, 2023
About this record
Access comprehensive regulatory information for Kubota blood cell volume measurement device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 63f850e611d454ec1831a85c6dcf62ca and manufactured by KUBOTA MFG. CORP. FUJIOKA PLANT. The authorized representative in Taiwan is DOUBLE EAGLE ENTERPRISE CO., LTD..
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