"Zhanyi" blood bank centrifuge for in vitro diagnosis (unsterilized)
Taiwan·Risk Class 1·SHINE ALPHA ELECTRONIC CO., LTD.·Registered Aug 14, 2020 – Aug 14, 2025Cancelled- Analysis ID
- 575c5d8e930109198513bf37a56af78d
- Manufacturer
- SHINE ALPHA ELECTRONIC CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JAN YI BIOTECH CO., 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
- 國產;; 委託製造;; QMS/QSD
- Registration Date
- Aug 14, 2020
- Expiry Date
- Aug 14, 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 "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 575c5d8e930109198513bf37a56af78d and manufactured by SHINE ALPHA ELECTRONIC 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 Tsinghua Electronics Co., Ltd.;; Zhanyi 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.