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"Will get" Shufeiya Fast Fluorescence Analyzer 2nd Generation (Unsterilized) - Taiwan Registration 79ca99b7cab90ac65db30c8380b7f09d

Access comprehensive regulatory information for "Will get" Shufeiya Fast Fluorescence Analyzer 2nd Generation (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 79ca99b7cab90ac65db30c8380b7f09d and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including QUIDEL 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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79ca99b7cab90ac65db30c8380b7f09d
Registration Details
Taiwan FDA Registration: 79ca99b7cab90ac65db30c8380b7f09d
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Device Details

"Will get" Shufeiya Fast Fluorescence Analyzer 2nd Generation (Unsterilized)
TW: "ๆœƒๅพ—" ่ˆ’ๅฆƒ้›…ๅฟซ้€Ÿ่žขๅ…‰ๅˆ†ๆžๅ„€ ็ฌฌไบŒไปฃ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

79ca99b7cab90ac65db30c8380b7f09d

DHA08401853803

Company Information

United States

Product Details

Limited to the classification and grading management measures of medical equipment "fluorescence instrument for clinical use (A.2560)" the first level identification range.

A Clinical chemistry and clinical toxicology

A.2560 Fluorometer for clinical use

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2025

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