QuickFly fluorescence analyzer (unsterilized)
Taiwan·Risk Class 1·QUIDEL CORPORATION·Registered Mar 12, 2013 – Mar 12, 2023Cancelled- Analysis ID
- 399835010640d7d11b51c668760f437a
- Customs Code
- DHA04401279802
- Manufacturer
- QUIDEL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BIO-CHECK LABORATORIES 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
- QMS/QSD;; 輸入
- Registration Date
- Mar 12, 2013
- Expiry Date
- Mar 12, 2023
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
Top companies providing products similar to "QuickFly fluorescence analyzer (unsterilized)"
Recently registered similar products
Access comprehensive regulatory information for QuickFly 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 399835010640d7d11b51c668760f437a and manufactured by QUIDEL CORPORATION. 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 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.