BEUDAMED
    132 results · 23ms · Sources: EU EUDAMED, US FDA

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    Livi Device

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694018128·MFx 2.0mm x 5mm Angulated Locking Standard Screw

    TMS SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036089528·

    ceraMotion®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011252005400·ceraMotion® Me Opaque A4, 40 g / dental ceramic...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197059565·Varady micro phlebextractor 17.0cm

    ceraMotion®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011252005200·ceraMotion® Me Opaque A4, 20 g / dental ceramic...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197173933·Tonsil needle straig...

    MONTAGE Settable, Resorbable Hemostatic Bone Putty

    FDA 510(k)
    FDA Unclassified ·Unknown

    R&R EXTERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    2.0MM SYSTEM PLATE 4 HOLE PLATE, STRAIGHT, MEDIUM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    2.0MM SYSTEM PLATE DOUBLE-Y-SHAPE, LONG

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·May 10, 2006

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·April 17, 2006

    SELOX ST 60

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.,·Product code LWS·December 2, 2005

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·October 25, 2005