BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    HOWMEDICE BONE PLUG

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

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123175·K-WIRE - SINGLE TROCAR THREADED 1.8mm DIA x 150mm

    N95 1860

    FDA Adverse Event
    Malfunction ·3M COMPANY·Product code MSH·January 11, 2021

    FLEXIBLE INTRODUCER CANNULA, MODEL 135-1837

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Infinity CentralStation Wide

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·December 22, 2025

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    ENDOPATH ETS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·November 29, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022