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

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    Altus Spine Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASAHI TREASURE FLOPPY PERIPHERAL GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BLOOD PRESSURE METER MODEL CH-101

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANK IMPL B9,5 D4,5 MM/L 9,5 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·October 30, 2023

    ANK C/X IMPL A11/D3.5/L11

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 11, 2022

    UNKNOWN ANKYLOS CX ABUTMENT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·August 18, 2025

    UNKNOWN ANKYLOS IMPLANT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·June 17, 2024

    UNKNOWN ANKYLOS ABUTMENT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·September 30, 2022

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 14, 2014

    ELECTROSURGICAL SNARE

    FDA Adverse Event
    Other ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDI·June 6, 2013

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·July 21, 2011

    ATLANTIS ABUTMENT TI

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 7, 2024

    UNKNOWN ANKYLOS CX TOOL

    FDA Adverse Event
    Malfunction ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 14, 2026

    UNKNOWN ANKYLOS CX ABUTMENT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·December 1, 2022

    UNKNOWN ANKYLOS CX ABUTMENT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·January 31, 2023

    T-HANDLE INSERTER

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·April 29, 2021

    LUCAS 3 CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024

    LUCAS 3 CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024

    ANK REG /X ABUT GH 1,5 A 0

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code NHA·August 23, 2024

    UNKNOWN ANKYLOS CX ABUTMENT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code NHA·February 10, 2025