"Shuofang" blood bank centrifuge for in vitro diagnostics (unsterilized)
- Analysis ID
- 8ba6175a722e85694bceab8a84bdd6a9
- Customs Code
- DHA08600233600
- Manufacturer Country
- China
- Authorized Representative
- AGREE HEALTH CARE TECHNOLOGY, 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
- Input;; QMS/QSD;; Chinese goods
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Shuofang" blood bank centrifuge for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ba6175a722e85694bceab8a84bdd6a9 and manufactured by HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT 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.