BEUDAMED
    25 results · 19ms · Sources: EU EUDAMED, US FDA

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    CARDIOX FLOW DETECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517574435·CoRoent Ant TLIF Ti, 12x12x40mm 0°

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020193·Perfect Fit™ II Pediatric Effort Belt Sensor, A...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702271423·Elvarex 3/Thigh High/Profile, Slant, Open Toe, ...

    CULLER IRIS SPATULA

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896013247·CULLER IRIS SPATULA CURVED WIDE BLADE STERLING ...

    G185

    FDA UDI
    RESEARCH INSTRUMENTS LIMITED·05060554120086·G185 Incubator for assisted reproduction

    G185

    FDA UDI
    RESEARCH INSTRUMENTS LIMITED·05060554120093·Incubator for Assisted reproduction

    COOK FETAL MEMBRANE MANIPULATOR, MODEL -FMM-122400

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

    SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYPHILIS HEALTH CHECK

    FDA 510(k)
    FDA Class 2 ·Microbiology

    KEEL

    FDA UDI
    The Wells Johnson Company·B458201224000·Cannula, Keel, specify length, diameter and han...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101757·L Tibial Baseplate Cemented Keeled Sz 4

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00732094210668·ProBP 2400 Blood Pressure Cuff, Large Adult (32...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100897·L Tibial Baseplate Cemented Stemmed Sz 4

    3I T3® TAPERED IMPLANT 4/3 X 11.5MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·May 20, 2025

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 19, 2025

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    LIFEPAK® 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019

    PROXIMATE PPH PROCEDURE SET

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 21, 2013

    MACH1 GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·September 26, 2014