BEUDAMED
    22 results · 30ms · Sources: EU EUDAMED, US FDA

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    VECTTOR VT-200

    FDA 510(k)
    FDA Class 2 ·Neurology

    Carriage adjustable R2R

    FDA UDI
    Liko AB·00887761981942·Overhead track patient lifting/transfer system

    LARGE CANNULATED SCREWS

    FDA UDI
    Smith & Nephew, Inc.·03596010064080·CANNULATED HIP PIN 70MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694055529·1.2mm Orbital Floor Plate, Fan, .3mm Thick

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528110782·1.2mm Orbital Floor Plate,Fan .3mm, SP

    SYNAPSE 3D BASIC TOOLS

    FDA 510(k)
    FDA Class 2 ·Radiology

    MAGLY 6.5MM CANNULATED SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 6, 2026

    COOK CELECT® PLATINUM NAVALIGN JUGULAR VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code DTK·November 17, 2016

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·March 25, 2025

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·January 14, 2020

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·November 14, 2025

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·July 15, 2025

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CRMD·Product code NIK·January 13, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·May 21, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 13, 2011

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·March 14, 2025

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·March 4, 2026

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·May 26, 2026

    Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139, K061525, K082374, K092140, K102388, K121062). Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superficial; Urology (including prostate); Transesophageal; Transrectal; Transvaginal; and Intraoperative (abdominal, thoracic, and vascular).

    FDA Recall
    Open, Classified ·GE Medical Systems, LLC·Product code ITX·November 10, 2022