BEUDAMED
    155 results · 33ms · Sources: EU EUDAMED, US FDA

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    PulmoVia Working Channel

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517566218·CoRoent Ant TLIF PEEK, 15x10x28mm 0°

    Oticon

    FDA UDI
    Oticon A/S·05707131284464·RIA2 PRO, MINIRITE 312 WL CBE DEMO

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036075194·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100097·BARRAQUER SPECULUM SOLID SMALL

    TiLock

    FDA UDI
    Genesys Orthopedics Systems LLC·M719G1502800·Pre-Bent Rod

    Alignment Rod Extension

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215057022·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197540438·Hypophysenspecula 80x9mm, 9mm 80mm

    GYNCARE MORCELLEX TISSUE MORCELLATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    RUNABOUT WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 7, 2014

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·May 30, 2013

    TRAPEZOID RX LITHOTRIPTER COMPATIBLE BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LQC·August 21, 2008

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 15, 2024

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 22, 2020

    CAPIOX FX05

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 21, 2020

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 1, 2022