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Duet®

MEDTRONIC PS MEDICAL, INC. · Model 46917 · UDI-DI 00763000406028

PCBJXGGWM Prescription
1
510(k) clearances
29
Adverse events
5
Recalls
6
Facilities

Description

EDMS 46917 DUET INTERLINK WITH LCATH

Recalls

DateFirmReason
2024-01-22Medtronic NeurosurgeryPotential for catheter disconnection from the patient line stopcock connectors.
2024-01-22Medtronic NeurosurgeryPotential for catheter disconnection from the patient line stopcock connectors.
2024-01-22Medtronic NeurosurgeryPotential for catheter disconnection from the patient line stopcock connectors.
2024-01-22Medtronic NeurosurgeryPotential for catheter disconnection from the patient line stopcock connectors.
2024-01-22Medtronic NeurosurgeryPotential for catheter disconnection from the patient line stopcock connectors.

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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.