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

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    Affixus(R) Natural Nail(R) System Humeral Nail

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Conventional Lead Apron .5mm Small 22 X 33

    FDA UDI
    Flow X Ray Corporation·00843696123024·Conventional Lead Apron .5mm Small, Teal

    GORNEY SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055803·GORNEY SCISSORS STRAIGHT DOUBLE BEVELED BLADES ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694060820·1.2mm Plating Module, ICON

    24M - Truckee Meadows Water - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588089140·24M - Truckee Meadows Water - Metal

    C-TEK MAXAN IMPLANTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWQ·May 15, 2009

    Astroglide Organix Liquid

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

    FINGER PULSE METER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIOMET PERITROCHANTERIC NAILING SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code HSB·August 6, 2009

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·March 31, 2012

    ESSURE

    FDA Adverse Event
    Other ·BAYER PHARMA AG·Product code HHS·March 31, 2009

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 25, 2009

    UNK DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 25, 2009

    UNK DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 25, 2009

    UNK DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 25, 2009

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 25, 2009

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 25, 2009

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·September 5, 2018

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·September 5, 2018

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·May 23, 2008