BEUDAMED
    13 results · 26ms · Sources: EU EUDAMED, US FDA

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    PRISMA DISPOSA. BRITE LITE FIBEROPTIC ENDO. W/PICK

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

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228750061·GC Initial™ IQ/Power Frame Modifier-Zr PFM-1

    AMC

    FDA UDI
    Advantage Medical Electronics, LLC·00849593004817·5 Lead GE to Draeger Single Pin Cable

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867263772·T15 HEXALOBE, ISO, SOLID

    CANTROL CK/MB CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SUN MEDICAL LAMINARIA CERVICAL DILATOR

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

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    UNKNOWN M2A HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 16, 2014

    ENRHYTHM DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·October 19, 2010

    *

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code LRY·December 13, 2012

    T15 HEXALOBE, ISO, CANN.

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 29, 2023

    G-WIRE W/TRCR TIP, THDD, 062"X9.25"

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code LXH·March 9, 2020

    COMPR FT SCRW, 5.0 LG, 40MM LGTH

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 9, 2020