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

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    BONART ART-P3II & P4 PIEZO ELECTRIC ULTRASONIC SCALER UNITS WITH ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Dental

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040090978·HOLLOW TUBING-CLEAR .030

    TRIDENT ACETABULAR SHELLS: PS-HA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO ACCU-CHEK ACTIVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CONNECTA PLUS3 WHITE PEGS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMG·November 19, 2024

    OMEGA-21 VERTEBRAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MNH·February 21, 2020

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    GOODBABY·Product code INM·April 16, 2013

    IBO BLADE, LEFT/RIGHT

    FDA Adverse Event
    Malfunction ·STRYKER IRELAND LTD.·Product code GFA·March 15, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 4, 2014

    ILIAC SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

    PEDICLE SCREW, UNKNOWN TYPE OR SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·August 30, 2021

    UNKNOWN LUMBAR IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code MNH·April 20, 2021

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025