"Shuofang" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT CO., LTD.·Registered Feb 26, 2015 – Feb 26, 2025Cancelled- Analysis ID
- 1f407417656f847a0c4d974b6aff7fce
- Customs Code
- DHA09600233606
- Manufacturer Country
- China
- Authorized Representative
- AGREE HEALTH CARE TECHNOLOGY, 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
- Chinese goods;; Input;; QMS/QSD
- Registration Date
- Feb 26, 2015
- Expiry Date
- Feb 26, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 1f407417656f847a0c4d974b6aff7fce 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.