BEUDAMED
    10,000 results · 42ms · Sources: EU EUDAMED, US FDA

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    PoNS

    FDA UDI
    Helius Medical, Inc·00864288000448·PoNS Controller

    PoNS

    FDA UDI
    Helius Medical, Inc·00864288000431·PoNS Mouthpiece

    PoNS

    FDA UDI
    Helius Medical, Inc·00864288000462·PoNS System

    Portable Neuromodulation Stimulator (PoNS)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Portable Neuromodulation Stimulator (PoNS)

    FDA 510(k)
    FDA Class 2 ·Neurology

    MD Orthopaedics

    FDA UDI
    MD ORTHOPAEDICS, INC.·00810060887325·Extra Short Bar 15°

    MD Orthopaedics

    FDA UDI
    MD ORTHOPAEDICS, INC.·00810060883648·Short Bar 10°

    MD Orthopaedics

    FDA UDI
    MD ORTHOPAEDICS, INC.·00810060887318·Extra Short Bar 10°

    MD Orthopaedics

    FDA UDI
    MD ORTHOPAEDICS, INC.·00810060883280·Long Bar 15°

    MD Orthopaedics

    FDA UDI
    MD ORTHOPAEDICS, INC.·00810060883655·Short Bar 15°

    MD Orthopaedics

    FDA UDI
    MD ORTHOPAEDICS, INC.·00810060883273·Long Bar 10°

    SURE LIFE

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODCUTS, LLC.·Product code DXN·August 30, 2018

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORK, LTD·Product code HCG·January 7, 2015

    MESH ¿ COMPOSIX L/P

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·April 23, 2020

    SURE LIFE

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODCUTS, LLC.·Product code DXN·July 3, 2018

    SURELIFE ARM BP MONITOR-PREMIUM

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODUCTS, LLC·Product code DXN·June 22, 2018

    WINGSPAN STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - FREMONT·Product code NJE·December 2, 2010

    ALTAIRE MR SYSTEM

    FDA Adverse Event
    Injury ·FUJIFILM HEALTHCARE CORPORATION·Product code LNH·March 8, 2022

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·September 1, 2017

    HIGH FREQUENCY OSCILLATORY VENTILATOR

    FDA Adverse Event
    Malfunction ·SENSORMEDICS CORP.·Product code LSZ·December 17, 1999