BEUDAMED
    23 results · 26ms · 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.

    FORTAFLEX SURGICAL MESH

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

    Healqu

    FDA UDI
    Healqu LLC·00819143020505·Healqu Hydroconductive Wound Dressing 4 x 5

    Flexi-Tip

    FDA UDI
    COOK INCORPORATED·00827002140165·Flexi-Tip Ureteral Catheter (Right)

    AOS ANTI-ROTATION SCREW 5.0mm x 105mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019933·

    Mimix QS

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036020811·

    OneTouch Ultra2

    FDA UDI
    LifeScan U.S. LLC·00353885008372·OneTouch Ultra2 Blood Glucose Monitoring Meter ...

    VERIDIAN

    FDA UDI
    VERIDIAN HEALTHCARE LLC·00845717000307·Provident Aneroid Sphygmomanometer, Thigh

    Flexi-Tip

    FDA UDI
    COOK INCORPORATED·00827002147980·Flexi-Tip, Ureteral Catheter (Right)

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967162294·ANGLED THORACIC SUPRALAMINAR HOOK, RIGHT, 10.5mm

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·July 21, 2005

    ESTEEM

    FDA Adverse Event
    Malfunction ·ENVOY MEDICAL CORPORATION·Product code OAF·December 10, 2021

    MOSS MIAMI 6.35MM ROD SYSTEM PEDICLE AND LAMINAR HOOKS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUTURTEK FASTCLOSE FASCIA CLOSURE DEVICE

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

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·October 28, 2019

    UNK GEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·October 19, 2021

    PORTEX SPINAL ANESTHESIA TRAYS

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC·Product code CAZ·March 15, 2013

    MAXCEM ELITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·March 16, 2011

    DEEP BRAIN STIMULATION

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 27, 2008

    IR 1200 Insulin Pump. IPX8 Rx only. Label P/N 400-125-00 Revision C.

    FDA Recall
    Terminated ·Animas Corporation·Product code LZG·September 28, 2004

    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