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

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    NATtrol BD MAX Vaginal Panel External Controls

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772344116·PROTECT.PRO ACTION BACK SUPPORT BLACK M

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489105633·PowerChem Neoprene Exam Gloves, Medium

    9014 DISPOSABLE NOSECLIPS

    FDA UDI
    HANS RUDOLPH, INC.·00874750004713·NOSE CLIP W/FOAM PADS DISPOSBL

    Zodiac

    FDA UDI
    ALPHATEC SPINE, INC.·00844856028845·PRE CONTOURED CP ROD 5.5 x 3cm NON-BROACHED

    10M - Southwest Gas Corp

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588010434·10M - Southwest Gas Corp

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383556248·"An absorbent paper points is an endodontic pap...

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383511407·"An absorbent paper points is an endodontic pap...

    SIGMA DIAGNOSTICS INFINITY GLUCOSE REAGENT, MODELS 17-25, 17-100P, 17-500P, 17-2000P, 18-20, 18-100P

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HA MALLORY/HEAD POROUS FEMORAL STEM & HA MALLORY/HEAD POROUS LATERALIZED FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALEUTIAN Interbody Systems

    FDA UDI
    VB Spine LLC·10888857189584·Straight Pituitary Rongeur Size 6 mm

    OMNIPOD DASH¿ INSULIN MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·June 2, 2020

    DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·December 14, 2015

    NAIMCO, INC., IONTOPHORESIS DRUG DELIVERY ELECTRODES, MODELS 201-400, 201-401, 201-402, 201-403 AND 201-405

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 26, 2013

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·August 3, 2011

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·July 24, 2008

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·March 30, 2023

    EVOLUT PRO PLUS VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 30, 2020

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 24, 2020