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"Will get" Shufeiya Fast Fluorescence Analyzer 2nd Generation (Unsterilized) - Taiwan Registration 155fdbfd79628de7d4f54b9963972b4b

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 155fdbfd79628de7d4f54b9963972b4b 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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155fdbfd79628de7d4f54b9963972b4b
Registration Details
Taiwan FDA Registration: 155fdbfd79628de7d4f54b9963972b4b
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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
Cancelled

Registration Details

155fdbfd79628de7d4f54b9963972b4b

DHA09401853802

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

Nov 23, 2017

Nov 23, 2022

Sep 30, 2021

Cancellation Information

Logged out

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