BEUDAMED
    22 results · 23ms · Sources: EU EUDAMED, US FDA

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    ClearMask Transparent Surgical Face Mask

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

    Avioq HTLV-I/II Microelisa System

    FDA UDI
    AVIOQ, Inc.·00853214004025·Avioq HTLV-I/II Microelisa System is a qualitat...

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825003265·Diagnostic EP Catheter, Damato curve, 10 electr...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776153915·MONO-POLAR CABLE BOVIE -RIGHT ANGLE CONNECTOR 1...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613121723·Monopolar RF-Cable, Right Angle Female Banana P...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180102958·MONOPOLAR RF-CABLE WITH RIGHT ANGLE FEMALE BANA...

    SafeOp

    FDA UDI
    ALPHATEC SPINE, INC.·00190376189147·Left stimulator cable

    VELOGENE GENOMIC IDENTIFICATIONASSAY FOR VRE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ELECSYS CORTISOL CALCHECK

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    T:SLIM G4 SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code OYC·May 30, 2019

    DEEP BRAIN STIMULATION DEVICES

    FDA Adverse Event
    MEDTRONIC NEUROMODULATION·Product code MHY·September 21, 2007

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

    DEEP BRAIN STIMULATION DEVICES

    FDA Adverse Event
    MEDTRONIC NEUROMODULATION·Product code MHY·September 21, 2007

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 24, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    TOTAL ASR ACET IMP SIZE 58

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 1, 2013

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 20, 2016

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·July 21, 2016

    MICROCLAVE CLEAR CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·June 5, 2014

    HARMONIC SCALPEL CURVED SHEAR (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·December 9, 2019