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CYSC

RANDOX LABORATORIES LIMITED · Model CYS4004 · UDI-DI 05055273208665

NDY Prescription
1
510(k) clearances
21
Adverse events
4
Recalls
24
Facilities

Description

The device is intended for the quantitative in vitro determination of Cystatin C in serum or plasma.

Recalls

DateFirmReason
2024-06-07Randox Laboratories Ltd.Cystatin C Reagent marketed without a 510 (k)
2024-02-14Randox Laboratories Ltd.Cystatin C Calibrator Series CVS 2699, is running with a negative bias compared to other methods
2020-09-02Gentian ASThe firm has identified lots of calibrators that have shown to measure incorrect high values over time compared to the assigned values when released for distribution. This could re
2018-03-05Tosoh Bioscience IncAsfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, depending upon the assay.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.