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

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    ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer, Straight Jaw, 37 cm Shaft Length

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

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446838036·SPECIAL, EMPOWR REV KNEE MONOBLOCK TIBIAL TRAY ...

    HHM

    FDA UDI
    Oticon A/S·05707131357489·G300 SC, MINIRITE R LI-ION 2.4G C058 HHM

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001713·CODMAN SLIM-LINE Aneurysm Clip 45 Degree Angle ...

    NA

    FDA UDI
    Synthes GmbH·10886982142627·2.4MM CORTEX SCREW 3.5MM HEAD/SELF-TAPPING 52MM

    20G SMA LASER FIBER, MODEL LF20; 25G SMA LASER FIBER, MODEL LF25

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

    MOTIONLOC SCREW FOR NCB POLYAXIAL LOCKING PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 28, 2013

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·October 27, 2014

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code OUT·October 12, 2016

    TAPERLOC 133 T1 PPS HO

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code OQG·March 25, 2020

    TAPERLOC XR T1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code OQG·March 25, 2020

    TAPERLOC 133 T1 PPS HO

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code OQG·March 25, 2020

    TAPERLOC XR T1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code OQG·March 25, 2020

    TAPERLOC XR T1 PPS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code OQG·March 25, 2020

    STEALTHSTATION S7 SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·December 8, 2016

    EVIS EXERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·June 22, 2016

    EVIS EXERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·June 22, 2016

    EVIS EXERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·June 22, 2016