"Kubota" Blood Bank Centrifuge for In Vitro Diagnostic Use (Non-Sterile)
Taiwan·Risk Class 1·MD·KUBOTA MFG. CORP. FUJIOKA PLANT·Registered Aug 24, 2018 – Aug 24, 2023Cancelled- Analysis ID
- 09db44d97831e92a856733fc2a174448
- License Form
- Ministry of Health Medical Device Import No. 019541
- Customs Code
- DHA09401954106
- Manufacturer
- KUBOTA MFG. CORP. FUJIOKA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- DOUBLE EAGLE ENTERPRISE CO., LTD.
- 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
- Aug 24, 2018
- Expiry Date
- Aug 24, 2023
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 09db44d97831e92a856733fc2a174448 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.