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"Will get" Shufeiya Rapid Fluorescence Analyzer (Unsterilized) - Taiwan Registration a1f8f931fca113ac703abfb6242e6f5d

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 a1f8f931fca113ac703abfb6242e6f5d 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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a1f8f931fca113ac703abfb6242e6f5d
Registration Details
Taiwan FDA Registration: a1f8f931fca113ac703abfb6242e6f5d
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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
Cancelled

Registration Details

a1f8f931fca113ac703abfb6242e6f5d

DHA04401303000

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

May 17, 2013

May 17, 2023

Sep 30, 2021

Cancellation Information

Logged out

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