BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Diode laser therapy device

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

    MODULAR PLUS HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VR MEDICAL HEAT AND MOISTURE EXCHANGER AND FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TRIDENT 0 DEG X3 INSERT 32MM HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 1, 2019

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN-BENNETT CORP.·Product code CBK·November 14, 2008

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 19, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 18, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025