"Will get" Shufeiya Fast Fluorescence Analyzer 2nd Generation (Unsterilized)
Taiwan·Risk Class 1·QUIDEL CORPORATION·Registered Nov 23, 2017 – Nov 23, 2022Cancelled- Analysis ID
- 155fdbfd79628de7d4f54b9963972b4b
- Customs Code
- DHA09401853802
- Manufacturer
- QUIDEL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
- 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
- Registration Date
- Nov 23, 2017
- Expiry Date
- Nov 23, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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.