BEUDAMED
    7 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 ×

    MTP DISPOSABLE TROCARS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ELECTROSURGICAL CUTTING/COAGULATION DEVICE/ACCESS

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

    SHARPLAN CO2 LAPAROSCOPIC PROBE MODEL 792 TO 792BX

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

    2520274-2013-10107

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MQN·February 27, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 16, 2011

    CARELINK

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    Accolade TMZF Plus Hip Stem: Catalog # 3020-0537 Accolate d TMZF Hip Stem # 5 Catalog #6020-3535 Accolade 132 Size 3.5 Catalog # 6021-0230 Accolade Plus TMZF Hip Stem #2 Catalog # 6021-0335 Accolade Plus TMZF Hip Stem #3 Catalog #3021-0435 Accolade TMZF Hip Stem #4 Catalog # 6021-0435 Accolade Plus TMZF Hip Stem #4 Catalog #6021-2530 Accolade (127 deg) Size 2.5 Accolade (127 deg) Size 2.5 Catalog # 6021-4535 Accolade (127 DEG) Size 4.5 K994366; k023105; K032300 Manufactured by " Stryker Ireland, Carrigtwohill Industrial Estate Carrington County Cork, Ireland The subject hip stem is a single-use device intended for the reconstruction of the head and neck of the femoral joint. This hip stem is intended for primary reconstruction of the proximal femur or revision total hip arthroplasty.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code ISL·March 1, 2011