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

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    PROFILE-ER

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04047872673174·LEVAMED STABILI-TRI ANK BLU R I

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099839·MD 1ST BI BD KT N/L UNIV 97

    SOFT-CUF

    FDA UDI
    GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.·00840682105576·SOFT-CUF, INFANT, 1 TB SCREW, 08 - 13 CM, SINGLE

    SYNCHRON LX SYSTEMS MICROALBUMIN CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SYNERGY HEAD/NECK COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERSLOK ANCHOR

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MAI·September 5, 2007

    NEXGEN PROLONG LPS-FLEX ARTICULAR SURFACE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·March 7, 2013

    UNKNOWN ZIMMER HIP

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code JDI·January 27, 2011

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 22, 2008

    METRX SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

    TECNIS SIMPLICITY

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code MFK·September 7, 2025

    45 MM LEFT STANDARD MANDIBLE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 8, 2014

    BENCHMARK 6F 071 DELIVERY CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·May 19, 2023

    The label (which is affixed to ScanPoint Communications Cradle) states: "...VERATHON ScanPoint Docking Station...Part No. 0570-0168...Bothell, WA USA..."

    FDA Recall
    Terminated ·Verathon, Inc.·Product code ITX·September 20, 2010

    TEMPOROMANDIBULAR JOINT SMALL LEFT FOSSA COMPONENT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 8, 2014

    SMALL RIGHT INVST FOSSA COMP

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 8, 2014

    TMJ SYSTEM CROSS DRIVE EMERGENCY FOSSA SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·May 3, 2018

    TMJ SYSTEM RIGHT STANDARD OFFSET MANIBULAR COMPONENT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·May 3, 2018

    "2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·May 3, 2018