Taiwan FDA registration bf8281137b6251010d6a0fbccf609cf5

"Zhanyi" blood bank centrifuge for in vitro diagnosis (unsterilized)

TW: “展億”體外診斷用血庫離心機(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Tsinghua Electronics Co., Ltd.;; Zhanyi Biotechnology Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
bf8281137b6251010d6a0fbccf609cf5
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
JAN YI BIOTECH CO., LTD.
Product details
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
委託製造;; 國產;; QMS/QSD
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for "Zhanyi" blood bank centrifuge for in vitro diagnosis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bf8281137b6251010d6a0fbccf609cf5 and manufactured by Tsinghua Electronics Co., Ltd.;; Zhanyi Biotechnology Co., Ltd. The authorized representative in Taiwan is JAN YI BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SHINE ALPHA ELECTRONIC 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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