BEUDAMED
    34 results · 29ms · Sources: EU EUDAMED, US FDA

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    MectaScope System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994625250·PLATE 7200067 ATL VISION ELITE 67.5MM

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00763000889890·PLATE 7200067 ATL VISION ELITE 67.5MM

    IBP Interface cable (BD/Ohmeda - Argon Medical)

    FDA UDI
    MIPM Mammendorfer Institut für Physik und Medizin GmbH·04255629200683·

    IBP Interface cable (BD/Ohmeda - Argon Medical)

    FDA UDI
    MIPM Mammendorfer Institut für Physik und Medizin GmbH·EMIP52000670·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694005944·1.6mm Screwdriver Shaft, Dental Latch

    24M - Memphis Light & Gas - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588000077·24M - Memphis Light & Gas - Metal

    Insurgical, Inc.

    FDA UDI
    Insurgical, Inc.·00860007230035·Oscillating Saw Packaged Assembly

    LEKSELL GAMMA KNIFE

    FDA Adverse Event
    Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 29, 2008

    LEKSELL GAMMA KNIFE

    FDA Adverse Event
    Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 29, 2008

    LEKSELL GAMMA KNIFE

    FDA Adverse Event
    Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 29, 2008

    LEKSELL GAMMA KNIFE

    FDA Adverse Event
    Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 29, 2008

    LEKSELL GAMMA KNIFE

    FDA Adverse Event
    Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 29, 2008

    LEKSELL GAMMA KNIFE

    FDA Adverse Event
    Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 29, 2008

    LEKSELL GAMMA KNIFE

    FDA Adverse Event
    Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 29, 2008

    GYRUS ENT SOMNOPLASTY GENERATOR

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

    ALKALINE PHOSPHATASE LIQUID REAGENT-KINETIC, MODELS A504-150 AND A504-500H

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BIOGX SARS-COV-2 OSR FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·May 13, 2020

    CSF-FLOW CONTROL VALVE, BURR HOLE, 12MM, MEDIUM PR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·October 15, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011