BEUDAMED
    32 results · 29ms · Sources: EU EUDAMED, US FDA

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    AUTOLOGEL PROCESS CENTRIFUGE, MODEL B4360 (100-103, 100-129)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Tornier Latitude

    FDA UDI
    TORNIER, INC.·00846832020201·SNAP-ON RADIAL TRIAL HEAD

    Humelock Reversed Shoulder

    FDA UDI
    FX SOLUTIONS·03701037306369·HUMELOCK REVERSED EPIPHYSEAL RASP Ø40mm

    Tiche PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481475029·

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981175092·Z-Rod, Dia. 5.5mm, Titanium, 340mm

    INCORPORATE

    FDA UDI
    SPINAL ELEMENTS·00840916126162·InCORPorate VBR Implant 40 W x 30 L x 34 H mm P...

    HYSTALOG HSG CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    OBC-149 BREAST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    Optetrak Logic

    FDA UDI
    Exactech, Inc.·10885862156730·TRIAL, CR FEMORAL, LOGIC®, RIGHT, SIZE 4

    Optetrak Logic

    FDA UDI
    Exactech, Inc.·10885862158130·

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWP·March 15, 2011

    PRECISION NOVI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 4, 2021

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·September 26, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·July 26, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·September 11, 2017

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 25, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 4, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 6, 2017

    GMRS TRL PROX FEM COMP STD

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·April 2, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 7, 2011