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

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    Quo-Test A1c System

    FDA 510(k)
    FDA Class 2 ·Hematology

    Bi-Metric XR-Series Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00880304650749·

    COMPREHENSIVE REVERSE SHOULDER

    FDA UDI
    Biomet Orthopedics, LLC·00880304475618·

    BONASTENT® Tracheal/Bronchial

    FDA UDI
    Sewoon Medical Co., Ltd.·08806369469128·

    THL1 LASER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CARDIOBLATE 68000 GNERATOR, BP2 SURGICAL ABLATION DEVICE, LP SURGICAL ABLATION DEVICE, GEMINI-SSURGICAL ABLATION DEVICE

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

    MOSAICMOD PROX HUM STM 8.5X100

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 19, 2020

    COMPREHENSIVE SHOULDER SYSTEM PRIMARY MINI LENGTH SHOULDER STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·March 8, 2017

    COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY WITH LOCKING RING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·April 13, 2017

    COMP RVRS SHLDR GLNSP STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 19, 2020

    ARCOM XL 44-36 STD HMRL BRNG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 19, 2020

    COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING/STANDARD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·April 13, 2017

    BD CONNECTA¿ STOPCOCK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·November 13, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 24, 2024

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 20, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 27, 2011

    ANCURE ENDOGRAFT

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·September 26, 2008

    ACROM XL 44-41 STD HMRL BRNG

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 17, 2017

    COMP RVRS SHLDR GLNSP STD 41MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 17, 2017