BEUDAMED
    10,000 results · 711ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MULTIflex LUX Coupling 465 LRN

    FDA UDI
    KaVo Dental GmbH·EKAV055315500·

    LANDMARK

    FDA UDI
    ZIEN MEDICAL TECHNOLOGIES, INC.·B090LRN0590·The LANDMARK REBOA catheter is intended for tem...

    UNKNOWN LIGASURE INSTRUMENT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 31, 2022

    SUTURE WIRE/LRN

    FDA Adverse Event
    Injury ·BROOKS MANUFACTURING SITE·Product code LRN·July 14, 2009

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·October 30, 2020

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·February 13, 2026

    NIM® EMG

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·February 13, 2026

    E-POLY 40MM HIWALL LRN SZ26

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 11, 2017

    E-POLY 40MM HIWALL LRN SZ26

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·April 20, 2016

    1.6MM KIRSCHNER WIRE W/TROCAR POINT 150MM

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code HTY·November 5, 2013

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 17, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 17, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 17, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 17, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 17, 2017

    2.0MM NON-COLORED THREADED GUIDE WIRE-SPADE POINT 230MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code LXT·March 14, 2017

    Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300; b. Quattro Drill 2.4mm, Hard Bone, Model Number CM-9324

    FDA Enforcement
    Class II ·Terminated·Cayenne Medical Inc.·August 8, 2018

    PRIMARY PLUMSET, CLAVE Y-SITE, NON-DEHP TUBING, 0.2 MICRON FILTER,

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·August 20, 2024

    TEGO® CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·January 9, 2024

    EVIS EXERA II XENON LIGHT SOURCE

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·October 1, 2022