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

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    TRUBLUE NASAL MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SOLED15-F

    FDA UDI
    ACEM SPA·08050705890347·SOLED15-F 1-ARM CEILING STANDARD LINE

    Tibial Nail 10mm x 40.5cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665029673·

    TMA - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989028270·TMA BROAD ARCH LO SML 0210 0250 PK/10

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450334850·

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529584719·Apex Tibial Nail Ø 11 x 405mm

    Leva® Anterior Expandable Spacer System

    FDA UDI
    Spine Wave, Inc.·10840642109122·Spacer, 30 mm (W) x 28 mm (D) x 15 mm (H), 15° ...

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K1104250·Tray, Base, 4.25", Arcamed

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K1104250·Tray, 4.25 Inch Base

    7230 ULTRASOUND IMAGING SYSTEM WITH TEI

    FDA 510(k)
    FDA Class 2 ·Radiology

    FORA G90 PERFORM BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TAPERLOC COMPLETE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 9, 2026

    TPRLC 133 MP TYPE1 BM SO 9.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 27, 2018

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 13, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·April 25, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 14, 2008

    TAPERLOC COMPLETE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 8, 2025

    BD INSULIN PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

    BACT/ALERT MP - 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·December 5, 2019

    Panorama Patient Monitoring Network. Cardiac Arrhythmia Monitor.

    FDA Recall
    Terminated ·Datascope Corp·Product code DRT·June 16, 2005