"Xuanjiang" in vitro diagnostic blood bank intelligent decapping centrifuge (unsterilized)
Taiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Feb 03, 2016 – Feb 03, 2026Cancelled- Analysis ID
- 0b47a06423c4e17c1010c63119bfa678
- Manufacturer
- LANNER BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LANNER BIOTECHNOLOGY 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, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- 國產;; QMS/QSD
- Registration Date
- Feb 03, 2016
- Expiry Date
- Feb 03, 2026
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Xuanjiang" in vitro diagnostic blood bank intelligent decapping centrifuge (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0b47a06423c4e17c1010c63119bfa678 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LANNER BIOTECHNOLOGY CO., LTD., 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.