"Xuanjiang" in vitro diagnostic blood bank intelligent decapping centrifuge (unsterilized)
Taiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 997d412cc1962f0b094dba0b252b23f2
- Manufacturer
- LANNER BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LANNER BIOTECHNOLOGY CO., LTD.
- 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
- Import Information
- 國產;; QMS/QSD
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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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 997d412cc1962f0b094dba0b252b23f2 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.