BEUDAMED
    33 results · 21ms · Sources: EU EUDAMED, US FDA

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    CAREVIEW 1800R

    FDA 510(k)
    FDA Class 2 ·Radiology

    Biomet® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00887868230820·

    BIOMET KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304232204·

    PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 6X40MM LOT. 1

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·December 13, 2019

    MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JMS SAFE WING CATH (SWC)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    M.U.S.T. POLYAXIAL PEDICLE SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025

    PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 6X30MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·May 14, 2024

    PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 7X35MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·March 10, 2021

    PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 6X35MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2023

    M.U.S.T. RODS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·March 31, 2026

    MYSPINE MC DRILL BASED GUIDE L05

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PQC·December 10, 2019

    MECTALIF OBLIQUE (TI PEEK) TIPEEK 10X24X10 L5°

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·June 25, 2024

    ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 5X40MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·January 10, 2024

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 12, 2019

    PEDICLE SCREW ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 5X40MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·July 25, 2023

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    HP MBT CEM KEEL PUNCH SZ 2-3

    FDA Adverse Event
    Malfunction ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LXH·October 4, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 1, 2011

    BD FACS¿ 7-COLOR SETUP BEADS 25 TESTS

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·November 28, 2022