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ISCUSflex

M DIALYSIS INC. · Model Clinical · UDI-DI 07332699000607

GWM
10
510(k) clearances
6,858
Adverse events (82 deaths)
52
Recalls
68
Facilities

Description

Microdialysis analyzer using substance specific reagents to evaluate the concentrations in the samples given by the Microdialysis sampling system (Catheter, 106 MD Pump and Microvials).

Recalls

DateFirmReason
2025-12-12Integra LifeSciences Corp. (NeuroSciences)Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
2025-12-12Integra LifeSciences Corp. (NeuroSciences)Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
2025-11-17SophysaCustomer complaints of Pressio monitor rebooting.
2024-11-01Medtronic NeurosurgeryDue to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS).
2024-11-01Medtronic NeurosurgeryDue to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS).
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak
2024-04-09Sophysa S.A.An increase in claims related to leakage of cerebrospinal fluid (CSF) from the proximal end of the catheter. In the event of a leak going undetected during implantation, it could p
2024-04-09Sophysa S.A.An increase in claims related to leakage of cerebrospinal fluid (CSF) from the proximal end of the catheter. In the event of a leak going undetected during implantation, it could p
2023-10-05Integra LifeSciences Corp.Firm is expanding the existing recall RES 90457 for the Cerelink, initiated in June 2022, to include all CereLink ICP Extension Cables. The updated corrective action includes a des

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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.