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

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    COULTER AMYLASE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978078823·CHANNEL 900-230 WORKING 12MM/6MM

    Mariner

    FDA UDI
    Seaspine Orthopedics Corporation·10889981129262·Head Inserter

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490002431·SPECIAL 12 X 6 WORKING CHANNEL

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978816913·SPECL 12MM/6MM WORKING CHANNEL

    Epatch Electrode-patch

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146EPE20·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197538466·Stille Ruskin Bone Rongeur, straight, 6m m 230mm

    HYFRECATOR

    FDA UDI
    Conmed Corporation·20653405031618·HYFRECATOR 2000 230 Volts AC - 50/60 Hz Electro...

    EXPEDIUM SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SMR REVER. LINER RETENTIVE STD

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code PHX·September 10, 2024

    HYFRECATOR

    FDA Adverse Event
    Injury ·CONMED·Product code GEI·April 8, 2026

    EVOLVE

    FDA Adverse Event
    Malfunction ·ARJOHUNTLIEHG, INC·Product code IKY·May 2, 2014

    HEMOCHRON SIGNATURE MICROCOAGULATION SYSTEM

    FDA Adverse Event
    Malfunction ·INTERNATIONAL TECHNIDYNE CORP.·Product code JPA·October 25, 2010

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 7, 2013

    SMR CONNECTOR SMALL STD

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·March 31, 2022

    HYFRECATOR

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·July 17, 2024

    HYFRECATOR 2000, 230V

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·December 17, 2020

    HYFRECATOR 2000, 230V

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·September 23, 2021

    HYFRECATOR 2000, 230V

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·April 17, 2023