BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    CAHSE AORTIC ROOT CANNULA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515251465·Lockwood Abdominal Demarcator w/ang hinge, 12 3...

    POWER FLOSS AND BRUSH EW 129 & EW 120

    FDA 510(k)
    FDA Class 1 ·Dental

    SAFETY NEEDLE SHEATH

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 15, 2013

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·July 11, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 19, 2011

    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. GXL NEUTRAL LINER, G0 28MM ID, 130-28-50; b. GXL NEUTRAL LINER, G00 22MM ID, 130-22-70; c. NOVATION GXL LIPPED LINER, G0 28MM ID, 132-28-50; d. NOVATION GXL LIPPED LINER, G00 22MM ID, 132-22-70;

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·September 21, 2022