BEUDAMED
    39 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SubtleHD (1.x)

    FDA 510(k)
    FDA Class 2 ·Radiology

    Flex

    FDA UDI
    Diversified Products, Inc.·00842894172902·

    TAPERLOC COMPLETE RASP/PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304632608·

    STRYKER PATIENT SPECIFIC POLYMER IMPLANT

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

    TaiChiC

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIKORAIL 142/243/250

    FDA Adverse Event
    Death ·HILL-ROM COMPANY/LIKO AB·Product code FSA·July 22, 2014

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 10, 2022

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 29, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 29, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 29, 2015

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·July 11, 2018

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·July 11, 2018

    LIKORALL 250 ES, NATURAL

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·November 24, 2014

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 7, 2008

    CURLIN INFUSION PAINSMART IOD IV PUMP

    FDA Adverse Event
    Malfunction ·MOOG MED DEVICES GROUP·Product code FRN·September 1, 2011

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    KENSTONE METAL·Product code IKX·July 23, 2013

    LIKORALL 242 ES, NATURAL

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·March 11, 2016

    LIKORALL 242 S, NATURAL

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·August 19, 2016

    Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likorall 200, 242, 243, 250, and LikoGuard L and XL.

    FDA Enforcement
    Class II ·Terminated·Hill-Rom, Inc.·November 9, 2016

    Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likorall 200, 242, 243, 250, and LikoGuard L and XL.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code FSA·August 9, 2016