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"Shuofang" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration 8ba6175a722e85694bceab8a84bdd6a9

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.

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8ba6175a722e85694bceab8a84bdd6a9
Registration Details
Taiwan FDA Registration: 8ba6175a722e85694bceab8a84bdd6a9
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Device Details

"Shuofang" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: "็ขฉๆ–น" ้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8ba6175a722e85694bceab8a84bdd6a9

DHA08600233600

Product Details

Limited to the classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.

B Hematology, pathology, and genetics

B.9275 Blood bank centrifuge for in vitro diagnostics

Input;; QMS/QSD;; Chinese goods

Dates and Status

Oct 01, 2021

Oct 31, 2025

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