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"Will get" Shufeiya Rapid Fluorescence Analyzer (Unsterilized) - Taiwan Registration a86bcca37aafe21fd8bb4b62f864d89a

Access comprehensive regulatory information for "Will get" Shufeiya Rapid Fluorescence 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 a86bcca37aafe21fd8bb4b62f864d89a 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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a86bcca37aafe21fd8bb4b62f864d89a
Registration Details
Taiwan FDA Registration: a86bcca37aafe21fd8bb4b62f864d89a
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Device Details

"Will get" Shufeiya Rapid Fluorescence Analyzer (Unsterilized)
TW: โ€œๆœƒๅพ—โ€่ˆ’ๅฆƒ้›…ๅฟซ้€Ÿ่žขๅ…‰ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a86bcca37aafe21fd8bb4b62f864d89a

DHA08401303007

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 (A2560)".

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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