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

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    G-PGD

    FDA UDI
    Vitrolife Sweden AB·07350025910185·

    G-PGD

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

    Smart Caregiver

    FDA UDI
    Smart Caregiver Corporation·00812293010532·Pager

    THE STRIPPER PGD

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

    STRIPPER

    FDA UDI
    ORIGIO INC.·00888937907933·STRIPPER PGD

    N/A

    FDA UDI
    ORIGIO INC.·00888937907834·STRIPPER PGD PLUNGER REPACEMENT

    PLATELET PGD TEST

    FDA Adverse Event
    Injury ·VERAX BIOMEDICAL INCOPORATED·Product code MZC·November 16, 2018

    VERAX PLATELET PGD TEST

    FDA Adverse Event
    Malfunction ·VERAX BIOMEDICAL INCORPORATED·Product code MZC·October 18, 2018

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·October 14, 2014

    STRIPPER

    FDA UDI
    ORIGIO INC.·00888937907940·STRIPPER PGD with Comfort Grip

    PGD-PRE-IMPLANTATION GENETIC DIAGNOSTIC PIPETTES (BIOPSY PIPETTES)

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

    VALITUDE CRT-P

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NKE·May 23, 2023

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 15, 2009

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 15, 2009

    UNK DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 15, 2009

    NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 27, 2012

    IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS)

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·May 12, 2016

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 21, 2011

    IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS)

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MRU·May 12, 2016

    ACCOLADE MRI DR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWP·April 18, 2023