"Kubota" Blood Bank Centrifuge for In Vitro Diagnostic Use (Non-Sterile)
Taiwan·Risk Class 1·MD·KUBOTA MFG. CORP. FUJIOKA PLANT·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- 07ee47f278591de9b5dfd1f958adee1a
- License Form
- Ministry of Health Medical Device Import Registration No. 019541
- Customs Code
- DHA08401954100
- Manufacturer
- KUBOTA MFG. CORP. FUJIOKA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- DOUBLE EAGLE ENTERPRISE CO., LTD.
- 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 and pathology devices
- Product Type (Level 2)
- B9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
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Access comprehensive regulatory information for "Kubota" Blood Bank Centrifuge for In Vitro Diagnostic Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 07ee47f278591de9b5dfd1f958adee1a and manufactured by KUBOTA MFG. CORP. FUJIOKA PLANT. The authorized representative in Taiwan is DOUBLE EAGLE ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KUBOTA MFG. CORP. FUJIOKA PLANT, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.