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

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    SYNTHETIC VINYL EXAMINATION GLOVES, POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    JOBST Bella Strong

    FDA UDI
    BSN MEDICAL, INC.·00035664009816·BELLA STRONG 20-30 MM HG ARMSLEEVE DOT BAND SIZ...

    AccuSITE™ Needle Guide

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436120002·Sterile needle guide with (14x147cm) CIV-flex c...

    BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    BAYER ADVIA IMS SYSTEM; C-REACTIVE PROTEIN SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    GMK-REVISION FEMUR REVISION PS SIZE 6 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 12, 2017

    GMK-HINGE FIXED TIBIAL TRAY SIZE 3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·August 28, 2019

    GMK HINGE FEMUR SIZE 5 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNAIONAL SA·Product code KRO·August 21, 2014

    GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 3 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 25, 2017

    GMK-REVISION FEMUR REVISION PS SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 19, 2019

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·February 25, 2020

    GMK HINGE FEMUR SIZE 2 RIGHT

    FDA Adverse Event
    Injury ·Product code KRO·September 12, 2014

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 29, 2025

    GMK-REVISION FEMUR REVISION PS SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 6, 2018

    GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 3+ RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 12, 2017

    KNIFE

    FDA Adverse Event
    Malfunction ·ALCON PRECISION DEVICE - SINKING SPRING·Product code HNN·April 30, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code FSA·September 19, 2014

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·May 18, 2011

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·November 6, 2019

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 30, 2019