BEUDAMED
    39 results · 31ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    RAPID PROGRAMMER

    FDA 510(k)
    FDA Class 2 ·Neurology

    COMPREHENSIVE SHOULDER SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304554122·

    Bernafon

    FDA UDI
    Bernafon AG·05711584058282·SPEAKER UNIT, 1 R MEDIUM

    Comprehensive® Shoulder System

    FDA UDI
    Biomet Orthopedics, LLC·00887868267611·

    5570 3L SYRINGE

    FDA UDI
    HANS RUDOLPH, INC.·00817136021225·5570 3L SYR HRI TOURQ 22/15mm

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·10840200301104·PELVIC EXAM TRAY

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013401104·PELVIC EXAM TRAY

    UROLOGY MONOPOLAR SNARE FOR TISSUE TRANSECTION

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

    HENKE SASS WOLF SAPHENOUS VEIN LAPAROSCOPE

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

    GLADIATOR¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·March 6, 2012

    IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 28, 2014

    ALIGN S SUPRAPUBIC URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED·Product code FTL·May 9, 2013

    ALARIS SE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·May 24, 2011

    MD HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 13, 2019

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSD·May 13, 2019

    PT HYBRID GLEN POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 13, 2019

    VERSA-DIAL 50X21X57 HUM HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSD·May 13, 2019

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·August 29, 2022

    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 11 MM, 55 MM Long Item Number: 113611

    FDA Recall
    Terminated ·Biomet, Inc.·Product code MBF·January 7, 2022

    Minor Lap Pack, Kit number AMS2624 convenience custom kits used for general surgery in hospital operating room

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·October 26, 2016