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"Taiyang" Wanlida Automatic Fluorescence Multiplex Analyzer (Unsterilized) - Taiwan Registration 0672e0ef813e44a1bd555bcf7c794d13

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 0672e0ef813e44a1bd555bcf7c794d13 and manufactured by LUMINEX CORPORATION. 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 DIASORIN INC., 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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0672e0ef813e44a1bd555bcf7c794d13
Registration Details
Taiwan FDA Registration: 0672e0ef813e44a1bd555bcf7c794d13
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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

0672e0ef813e44a1bd555bcf7c794d13

DHA04401200700

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

Input;; QMS/QSD

Dates and Status

Aug 01, 2012

Aug 01, 2017

Dec 20, 2019

Cancellation Information

Logged out

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