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

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    INNOVASIVE DEVICES ROTATOR CUFF FASTNER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIED

    FDA 510(k)
    FDA Class 2 ·Radiology

    TANDEM(R) M-PAK(TM) PAP IMMUNOENZYMETRIC ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CA-1000

    FDA Adverse Event
    Injury ·TOA MEDICAL ELECTRONICS·Product code GKP·January 6, 1997

    PERFORMER INTRODUCER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·September 24, 2015

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    G4 PLATINUM PEDIATRIC CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 29, 2014

    THORATEC® HEARTMATE 3¿ VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·July 28, 2025

    THORATEC® HEARTMATE 3¿ VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·May 7, 2025

    PERFORMER INTRODUCER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·April 28, 2017