23 results · 21ms · Sources: EU EUDAMED, US FDA

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Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide Product Code: ASK-04020-PMC The Arrow Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels.

FDA Recall
Open, Classified ·Arrow International Inc·Product code DQX·December 12, 2019

ADVANTA VXT, 8X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 8X40, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 8X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 8X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 8X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 5-8X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 6X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 6X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 7X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 7X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 7X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 8X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024

ADVANTA VXT, 8X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DSY·May 3, 2024