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

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    MRidium 3860+ MRI infusion Pump/ Monitoring System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·10840200302095·SINGLE INSTRUMENT

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013402095·SINGLE INSTRUMENT

    VAULT ALIF SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERVEX-BRUSH COMBI

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

    NEXGEN PROVISIONAL ARTICULAR SURFACE

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HWT·February 26, 2020

    CADD-MS 3 AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL·Product code FRN·May 24, 2013

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·June 29, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 10, 2015

    VANGUARD MONO FINNED STM TIB 71X14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JWH·December 9, 2024

    VANGUARD ROCC TIB BRG UHMWPE 60X10MM

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JWH·September 16, 2025