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Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·November 4, 2015

MULTIGENT Creatinine (Enzymatic), Catalog Numbers 8L24-31 and 8L24-41; IVD. Intended for the quantitative determination of creatinine in human serum, plasma, and urine using the ARCHITECT c Systems The product is a medical device (chemistry reagent) and is intended for the quantitative determination of creatinine in human serum, plasma, and urine using the ARCHITECT c Systems. The kit is provided as a ready to use liquid material consisting in two components: Reagent 1 and Reagent 2. According to the catalogue number, the kit is composed of three vials of 48 ml for Reagent 1 and three vials of 18 ml for Reagent 2 in the configuration 8L24-31. The configuration 8L24-41 consists in ten vials of 90 ml for Reagent 1 and ten vials of 34 ml for Reagent 2

FDA Enforcement
Class II ·Terminated·Sentinel CH SPA·August 9, 2017

Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·October 2, 2019

MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 8L25-30

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·October 2, 2019

Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of the Alinity c CRP Vario assay, Cardiac CRP high sensitivity method [Cardiac CRP], on the Alinity c analyzer.

FDA Enforcement
Class III ·Terminated·Sentinel CH SpA·October 13, 2021

IRON assay, Reference Numbers 6K95-41 and 6K95-30

FDA Enforcement
Class II ·Ongoing·Sentinel CH SpA·November 29, 2023

Alinity c Iron Reagent, Reference Number 08P3920

FDA Enforcement
Class II ·Ongoing·Sentinel CH SpA·November 29, 2023

ACE Control Set - IVD Control set for the quantitative determination of Angiotensin Converting Enzyme (ACE) REF 1667001

FDA Enforcement
Class III ·Ongoing·Sentinel CH SpA·July 14, 2021