BEUDAMED
    12 results · 40ms · Sources: EU EUDAMED, US FDA

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    PHILIPS ESSENTA DR

    FDA 510(k)
    FDA Class 2 ·Radiology

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496070528·BE YOU TONIC CURVY PRO, SIZE S-XL, BLU TONIC, G...

    TITANIUM CEMENT RESTRICTOR MATERIAL PEEK

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

    ACCUCLOT DRVVT CONFIRM, CATALOG NO. A62119

    FDA 510(k)
    FDA Class 1 ·Hematology

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 22, 2021

    STELLARIS 23GA POSTERIOR PACK W AFI & WF

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·April 17, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·March 29, 2011

    ONE TOUCH ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·July 2, 2008

    G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·January 1, 2014

    KYPHON KURVE BONE FILLER DEVICE 13GA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code KIH·July 14, 2020

    GIANTURCO-ROEHM BIRD'S NEST JUGULAR VENA CAVA FILTER

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·March 25, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·March 23, 2018