BEUDAMED
    10 results · 21ms · 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.

    JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    STERILE BRIGHTWAY BRAND POWER-FREE, LATEX EXAMINATION GLOVES, WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS) TESTED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SPATOUCH PHOTOEPILATION SYSTEM

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

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·October 2, 2009

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 25, 2025

    27 G X 1/2 IN. BD PRECISIONGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·November 5, 2017

    PRIME ZOOM STRETCHER, 30"LITTER

    FDA Adverse Event
    Other ·STRYKER MEDICAL·Product code INK·May 5, 2011

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIM·May 2, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·September 15, 2014

    BD PRECISIONGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·May 22, 2018