BEUDAMED
    19 results · 24ms · Sources: EU EUDAMED, US FDA

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    UTERMOHLEN CRYO PROFESSIONAL

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814664·GENUMEDI SILVER SIZE III

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551057582·Ear Hook, ball end, size 3

    Trial Cups

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215038946·

    AURA 70 WATT BIPOLAR ELECTROSURGICAL COAGULATORS, MODELS 28-2000 AND 28-2600

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

    CHEMTRUE SINGLE / MULTI DRUG SCREEN CASSETTE / DIP CARD TESTS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ONE TOUCH ULTRASMART

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 18, 2003

    BD Q-SYTE CLOSED LUER ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·May 21, 2025

    ZEPHYR XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

    25G BI-B POSTERIOR ELITE W WF

    FDA Adverse Event
    Injury ·BAUSCH + LOMB, INC.·Product code HQC·September 3, 2021

    25G BI-B POSTERIOR ELITE W WF

    FDA Adverse Event
    Injury ·BAUSCH + LOMB, INC.·Product code HQC·September 3, 2021

    25G BI-B POSTERIOR ELITE W WF

    FDA Adverse Event
    Injury ·BAUSCH + LOMB, INC.·Product code HQC·September 3, 2021

    25G BI-B POSTERIOR ELITE W WF

    FDA Adverse Event
    Injury ·BAUSCH + LOMB, INC.·Product code HQC·September 3, 2021

    #7 PE ZIPLOOP EXT TOGGLELOC

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·April 4, 2019

    5095 SURGICAL TABLE

    FDA Adverse Event
    Malfunction ·STERIS CORPORATION - MONTGOMERY·Product code FQO·February 23, 2024

    4085 SURGICAL TABLE

    FDA Adverse Event
    Malfunction ·STERIS CORPORATION - MONTGOMERY·Product code FQO·March 28, 2018

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023