Taiwan FDA registration a1f8f931fca113ac703abfb6242e6f5d

"Will get" Shufeiya Rapid Fluorescence Analyzer (Unsterilized)

TW: “會得”舒妃雅快速螢光分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·QUIDEL CORPORATION·Registered May 17, 2013 – May 17, 2023Cancelled
Registration details
Analysis ID
a1f8f931fca113ac703abfb6242e6f5d
Customs Code
DHA04401303000
Company information
Manufacturer
QUIDEL CORPORATION
Manufacturer Country
United States
Authorized Representative
GRAND MARQUIS CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Fluorescence Instrument for Clinical Use (A2560)".
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2560 Fluorometer for clinical use
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
May 17, 2013
Expiry Date
May 17, 2023
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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