BEUDAMED
    22 results · 39ms · Sources: EU EUDAMED, US FDA

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    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NIO·March 4, 2025

    Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code DQY·February 7, 2025

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code DQO·November 7, 2022

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code MGB·November 28, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code DQO·September 26, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NTE·March 24, 2023

    Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code NIO·March 4, 2025

    MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code MGB·November 28, 2023

    PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX, PG3990BPS, PG3990BPX.

    FDA Recall
    Open, Classified ·Cordis US Corp·Product code FGE·May 20, 2022