BEUDAMED
    25 results · 22ms · Sources: EU EUDAMED, US FDA

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    Dosis SAM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BI-METRIC XR-SERIES HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304650558·

    Maestro™ Total Wrist

    FDA UDI
    Biomet Orthopedics, LLC·00887868239885·

    MAESTRO TOTAL WRIST

    FDA UDI
    Biomet Orthopedics, LLC·00880304555051·

    FUKUSHIMA SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896000377·FUKUSHIMA SUCTION TUBE

    FUKUSHIMA SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B0991804100·FUKUSHIMA SUCTION TUBE

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·May 9, 2018

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973107019·TRIAL 90-SRK-180410 POLY PS 4X10MM

    PIEZOELECTRIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·May 8, 2018

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 20, 2013

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 27, 2011

    GMK-SPHERE 02.07.1204R TIBIAL TRAY FIXED CEMENTED SIZE 4 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·February 12, 2025

    BD VACUTAINER® 9NC 0.109M BUFFERED TRISODIUM CITRATE PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 31, 2023

    X31-400010 578440 EXACT/ ALLIANCE BROACH PROVISIONAL 10X 130MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HWT·June 5, 2017

    BI-METRIC XR-SERIES HIP SYSTEM FEMORAL STEM 131.5 NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·June 6, 2017

    X31-400009 132940 EXACT/ ALLIANCE BROACH PROVISIONAL 9MM X 125MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HWT·June 5, 2017

    BIOZORB

    FDA Adverse Event
    Injury ·HOLOGIC, INC·Product code NEU·September 5, 2023