BEUDAMED
    23 results · 35ms · Sources: EU EUDAMED, US FDA

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    MICRO-AIRE STERNUM SAW 4800

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Arthrex®

    FDA UDI
    ARTHREX, INC.·10888867052113·GUIDE WIRE, TROCAR TIP, 1.35 MM

    PLEUR-EVAC II AUTOTRANSFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    THROMBOLYTIC ACTIVITY TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 23, 2014

    CONQUEST PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·November 4, 2010

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 16, 2012

    LOW PROF SCRW,SS 4.0X 45MMCANN,SHT THD

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·September 27, 2023

    DRV SFT,CANN,QC,T15 HEXALOBE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·September 27, 2023

    LO-PRO SCRW,TI,3.0MMX 20MMCORT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 16, 2023

    LO-PRO SCRW,TI,3.5MMX 12MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·August 17, 2023

    3.0 X 14MM VAL SCREW, TI

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

    3.0 X 16MM VAL SCREW, TI

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

    3.0 X 18MM VAL SCREW, TI

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

    LOCKING DISTAL FIBULA PLATE, TI ,LEFT,4H

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·August 17, 2023

    3.0 X 20MM VAL SCREW, TI

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

    QCKFIX SCRW,TI,CANN ST,CANC.,4.0X 52MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWC·August 16, 2023

    LO-PRO SCRW,TI,3.5MMX 26MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

    K-LESS T-ROPE W/DRV, SYN REPR, TI

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HTN·August 16, 2023

    LO-PRO SCRW,TI,3.5MMX 14MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023