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"Zhanyi" blood bank centrifuge for in vitro diagnosis (unsterilized) - Taiwan Registration 575c5d8e930109198513bf37a56af78d

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.

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575c5d8e930109198513bf37a56af78d
Registration Details
Taiwan FDA Registration: 575c5d8e930109198513bf37a56af78d
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Device Details

"Zhanyi" blood bank centrifuge for in vitro diagnosis (unsterilized)
TW: โ€œๅฑ•ๅ„„โ€้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

575c5d8e930109198513bf37a56af78d

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.

B Hematology, pathology, and genetics

B.9275 Blood bank centrifuge for in vitro diagnostics

ๅœ‹็”ข;; ๅง”่จ—่ฃฝ้€ ;; QMS/QSD

Dates and Status

Aug 14, 2020

Aug 14, 2025

Sep 30, 2021

Cancellation Information

Logged out

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