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

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    Venner PneuX™ TT (Tracheostomy Tube) Size 7.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 8.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 9.0 mm

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VERTE-STACK® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074520612·SPACER 9192511 CRESCENT PEEK 25X11

    Echo® Bi-Metric® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868273940·

    Echo® Press-Fit Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868260865·

    ECHO BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304462878·

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198741·AK3 Ultra Insert Trial Size 5, 11mm

    Symetri Clear

    FDA UDI
    ORMCO CORPORATION·00889989082999·U4&5L SYMETRI CLEAR MCLAUGHLIN, BENNETT & TREVI...

    M2A-MAGNUM MOD HD SZ 44MM 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 3, 2025

    M2A-MAGNUM MOD HD SZ 44MM 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 3, 2025

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780479024·Integra® Miltex® House Obtuse Pick, 6-1/4", 0.2...

    DOBBHOFF DUAL PORT FEEDING TUBE

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

    MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 22, 2025

    CER BIOLOXD MOD HD 32MM STD NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 7, 2019

    MYNX ACE 6F/7F VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·ACCESSCLOSURE, INC.·Product code MGB·October 22, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 5, 2011

    STERNAL ZIPFIX W/NEEDLE PEEK 5U

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDQ·June 27, 2013

    CER BIOLOXD MOD HD 32MM STD NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 22, 2020

    M2A-MAGNUM 42-50 TPR INSRT STD 0/0MMT1

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·April 3, 2025

    M2A-MAGNUM 42-50 TPR INSRT STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 16, 2026