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"Taiyang" Wanlida Automatic Fluorescence Multiplex Analyzer (Unsterilized) - Taiwan Registration 0eddc209d7a1c1e58a344088057a8e57

Access comprehensive regulatory information for "Taiyang" Wanlida Automatic Fluorescence Multiplex Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0eddc209d7a1c1e58a344088057a8e57 and manufactured by DIASORIN INC.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LUMINEX CORPORATION, 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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0eddc209d7a1c1e58a344088057a8e57
Registration Details
Taiwan FDA Registration: 0eddc209d7a1c1e58a344088057a8e57
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Device Details

"Taiyang" Wanlida Automatic Fluorescence Multiplex Analyzer (Unsterilized)
TW: "ๅคชๆš˜" ่ฌๅˆฉ้”ๅ…จ่‡ชๅ‹•่žขๅ…‰ๅคš้‡ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0eddc209d7a1c1e58a344088057a8e57

DHA04401097909

Company Information

United States

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Fluorescence Instrument for Clinical Use (A.2560)".

A Clinical chemistry and clinical toxicology

A.2560 Fluorometer for clinical use

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 27, 2011

Oct 27, 2016

Oct 08, 2012

Cancellation Information

Logged out

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