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

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    Focus 43C detector, TRIMAX 43C detector

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772412488·PROTECT.LUMBOSTYLE BACK SUPPORT BLACK II

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00142006220·CC-102

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034616·Single Compartment Case

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540256942·SCREWDRIVER BLADE, 2.0MM HEX-FIT

    ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000); ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; AND WANDS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAIL HOLDING SCRE WGAMMA3 8X35MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 21, 2012

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·November 1, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·November 1, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·November 1, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·November 1, 2019

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·January 20, 2010

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·January 20, 2010

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·January 28, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·January 28, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·January 28, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·January 28, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·January 28, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·January 28, 2008