BEUDAMED
    52 results · 24ms · Sources: EU EUDAMED, US FDA

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    N LATEX IGM

    FDA 510(k)
    FDA Class 2 ·Immunology

    AOS CANCELLOUS LAG SCREW 4.0mm x 14mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665009415·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0120140·Screwdriver, Polyaxial, Standard, Cannulated, L...

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967187495·Battalion, LLIF Trial, 15°, 20 mm Wide, 14 mm X...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710620320140·Quad Channel Met-Traverse, 32mm x 14mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710810320140·Dwyer Calcaneal Guide, 32mm x 14mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710820320140·Zadik Calcaneal Guide, 32mm x 14°

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710300320140·Tibial Osteotmy Guide, 32mm x 14mm

    TMC PSI Cut Guide System

    FDA UDI
    Treace Medical Concepts, Inc.·00810111222327·Cut Guide

    VIANOX DELIVERY SYSTEM, MODEL I

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MODIFICATION TO BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ID CORE XT

    FDA Adverse Event
    Malfunction ·PROGENIKA BIOPHARMA S.A.·Product code PEP·February 7, 2020

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 26, 2013

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 28, 2011

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·April 21, 2008

    HEARTSINE SAMARITAN 350P AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·March 13, 2018

    PACKAGE,500P,PP03,INTL EN,500-BAS-SP-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·November 6, 2018

    PACKAGE,350P,PP03,IT,350-BAS-IT-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·October 29, 2018

    PACKAGE,350P,PP03,DE,350-BAS-DE-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·July 30, 2018

    PACKAGE, 350P, PP03J, JA, 350-BAS-JA-08

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·December 17, 2018