Taiwan FDA registration 8560815eab5bc223a80b40246a6e0fe6

QuickProfit Expert Fluorescence Analyzer (Unsterilized)

TW: 快得利 揣耶濟 專家型螢光分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Quidel Cardiovascular Inc.·Registered Jun 17, 2019 – Jun 17, 2024Cancelled
Registration details
Analysis ID
8560815eab5bc223a80b40246a6e0fe6
Customs Code
DHA09402055800
Company information
Manufacturer Country
United States
Authorized Representative
BIO-CHECK LABORATORIES 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 (A.2560)".
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
Jun 17, 2019
Expiry Date
Jun 17, 2024
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 QuickProfit Expert 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 8560815eab5bc223a80b40246a6e0fe6 and manufactured by Quidel Cardiovascular Inc.. The authorized representative in Taiwan is BIO-CHECK LABORATORIES LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Quidel Cardiovascular Inc., 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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