BEUDAMED
    532 results · 20ms · Sources: EU EUDAMED, US FDA

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    VECTRA LASER SYSTEM

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

    Integra®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780088394·Integra® Netterville Window Template

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA UDI
    FX SOLUTIONS·03701037311981·REAMER Ø14 mm / HUDSON

    Claymount

    FDA UDI
    Varex Imaging Nederland B.V.·08718755000771·x-ray beam-limiting device, to restrict the dim...

    Entuit Gastrostomy BR Balloon Retention Feeding Tube with ENFit Connection

    FDA UDI
    XERIDIEM MEDICAL DEVICES, INC.·00827002447813·Entuit Gastrostomy BR Balloon Retention Feeding...

    ACUVUE 2 BRAND (ETAFILCON A) CONTACT LENS, WITH UV BLOCKER TINTED (TO MASK OR ENHANCE THE NATURAL IRIS COLOR)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    RS-4M+MUSCLE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 20, 2013

    SOFTCLIX PLUS LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·June 10, 2008

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·April 15, 2011

    NEEDLE 25X1 RB

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·January 8, 2025

    2.5 mm Reaming Rod W/Ball Tip 650 mm, Sterile

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·November 30, 2016

    NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026

    NEEDLE 25X1 RB

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·December 13, 2024

    NEEDLE 25X1 RB

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·December 23, 2024

    NEEDLE 25X1 RB

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·December 23, 2024

    PANEL PHOENIX NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026