BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION

    FDA 510(k)

    Malibu

    FDA UDI
    Seaspine Orthopedics Corporation·10889981081119·Tap 8.0mm, Modular (for 8.5mm Screw)

    THERMO PAL INFRARED EAR THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANGELTOUCH VENTED IV ADMINISTRATION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·January 11, 2013

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·November 17, 2010

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 3, 2014

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021