BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    ASPIRATOR

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

    COOK FIVE LUMEN CENTRAL VENOUS CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AIXPLORER

    FDA 510(k)
    FDA Class 2 ·Radiology

    R-PILOT, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·June 4, 2024

    R-PILOT, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·August 9, 2024

    R-PILOT, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·June 4, 2024

    R-PILOT, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·June 4, 2024

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·May 27, 2014

    PULL REDUCTION DEVICE FOR 4.3MM PERCUTANEOUS DRILL GUIDE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·November 14, 2012

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 10, 2015