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

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    VitalBeam

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768505·GENUMEDI PSS GREEN VI

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699588·GENUMEDI PSS BLUE, SIZE VI

    Oticon

    FDA UDI
    Oticon A/S·05707131280732·NERA2 PRO, BTE 13 WL 100 CNB

    Healthweigh

    FDA UDI
    Rice Lake Weighing Systems, Inc.·00850042373088·Scale, SB-1150 1000 LB. Package (Scale, Ramp an...

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100189·MCINTYRE SPECULUM CLOSED WIRE

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171028635·PESSARY, HODGE #3, W/O SUPPORT, 80mm

    VENUS BASIC SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HARMONY PORT SYSTEM, MODEL 1907 SERIES

    FDA 510(k)
    FDA Class 2 ·Neurology

    VERCISE CARTESIA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·April 1, 2024

    VERSACROSS CONNECT LAAC ACCESS SOLUTION

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

    ITREL 3

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 6, 2013

    VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HAV IGM REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LOL·July 6, 2011

    VERSACROSS ACCESS SOLUTION

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·April 19, 2023

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI, INC.·Product code EGS·July 21, 2015

    VERSACROSS ACCESS SOLUTION

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DYB·April 20, 2023

    VERSACROSS CONNECT LAAC ACCESS SOLUTION

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·April 25, 2023

    MISAGO RX Self Expanding Peripheral Stem

    FDA Enforcement
    Class II ·Terminated·Terumo Medical Corp·December 7, 2016

    Conmed System 2500 Electrosurgical Unit, REF 60-8011-SYS, Conmed Corporation

    FDA Recall
    Terminated ·Conmed Electrosurgery·Product code GEI·September 5, 2006