BEUDAMED
    29 results · 24ms · Sources: EU EUDAMED, US FDA

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    MODIFIED MERCI RETRIEVER, MODEL 90060

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049194·K-Wires, Single trocar, .045-inch (1.1mm) diame...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292862·

    K-Wire w. trocar/round end 1.14mm/127mm, 6 pcs./unit

    FDA UDI
    mahe medical gmbh·EMAHKM711720·K-Wire w. trocar/round end 1.14mm...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659484405·K-Wire w. trocar/round end _x000D_...

    ARTHREX BIO-TRANSFIX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POLYESTER NONABSORBABLE SURGICAL SUTURES URP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INFINION CX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 14, 2023

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·April 8, 2013

    MINI TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·April 27, 2011

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 10, 2008

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 22, 2025

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 5, 2022

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 16, 2022

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 24, 2022

    CAPIOX FX05 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·May 19, 2023