BEUDAMED
    33 results · 29ms · Sources: EU EUDAMED, US FDA

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    The Trevo Trak 21 Microcatheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker(s) on the distal end and a luer hub on the proximal end. The catheter shaft has a hydrophilic coating on the distal 100cm to reduce friction during use. The radiopaque shaft and distal marker(s) facilitate fluoroscopic visualization. A rotating hemostatic valve with side-arm adapter is provided with each microcatheter.

    FDA Recall
    Open, Classified ·Stryker Neurovascular·Product code QJP·August 30, 2024

    Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm

    FDA Recall
    Open, Classified ·Stryker, Inc.·Product code DQO·December 6, 2023

    Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm

    FDA Recall
    Open, Classified ·Stryker, Inc.·Product code QJP·December 6, 2023

    Guider Softip Guide Catheter 6F 100CM MULTI PURPOSE, Catalog number M003101460, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM, Catalog number M003101430, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM, Catalog number H965100430, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE, Catalog number M003100630, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 8F 90CM MULTI PURPOSE, Catalog number H965100480, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM, Catalog number M003101420, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 8F PRE-SHAPED 40 100CM, Catalog number M003101440, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 6F 90CM MULTI PURPOSE, Catalog number H965100460, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE, Catalog number H965100470, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 5F 100CM MULTI PURPOSE, Catalog number M003101630, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 5F PRE-SHAPED 40 100CM, Catalog number M003101620, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 7F 100CM MULTI PURPOSE, Catalog number M003101470, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM, Catalog number H965100440, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 8F 100CM MULTI PURPOSE, Catalog number M003101480, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    Guider Softip Guide Catheter 5F PRE-SHAPED 40 90CM, Catalog number M003100620, cardiac guide catheter

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code DQY·July 27, 2023

    INZONE DETACHMENT SYSTEM, REF: M00345100950

    FDA Recall
    Open, Classified ·Stryker Neurovascular·Product code HCG·April 6, 2026