BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Asahi PTCA Guide Wire Asahi SION Series

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PALM-PRO POWDER FREE NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BLUE POWER FREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BD KIESTRA IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025

    BONE SCREW, CROSS-PIN, DIAM.2.3X16MM, STERILE, (1/PACKAGE)

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code JEY·June 26, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MED SYSTEMS, INNOVATION CENTER - SILICONE VALLEY·Product code GEX·June 7, 2011

    COHERENCE THERAPIST

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS·Product code IYE·September 19, 2008