BEUDAMED
    10 results · 20ms · 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 ×

    EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODULAR FLEXIBLE REAMER HEAD, Ø9.0mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665000856·

    INFINION 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 29, 2024

    Diode Laser Hair Removal

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

    Back 3 COLOR

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

    FLEXIBLE REAMER SHAFT, NITINOL, HUDSON

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·February 20, 2023

    MODULAR FLEXIBLE REAMER HEAD, Ø9.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·February 20, 2023

    PARIETEX UGYTEX PP ANTERIOR KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·August 29, 2011

    CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNT·November 4, 2008

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES INC.·Product code FTM·July 16, 2013