BEUDAMED
    1,269 results · 29ms · 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 FDA Adverse Event ×

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·February 12, 2021

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 24, 2012

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 8, 2021

    COVER, MATTRESS (MEDICAL PURPOSES)

    FDA Adverse Event
    Malfunction ·SEG-MAX/DERBY INDUSTRIES.·Product code FMW·January 6, 2025

    COVER, MATTRESS (MEDICAL PURPOSES)

    FDA Adverse Event
    Malfunction ·SEG-MAX/DERBY INDUSTRIES.·Product code FMW·January 6, 2025

    SEG

    FDA Adverse Event
    Malfunction ·ZIMMER·Product code DZE·July 3, 2025

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 1, 2012

    ARTHROCARE INC.

    FDA Adverse Event
    Malfunction ·ARTHROCARE INC.·Product code HRX·April 22, 2003

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 10, 2012

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 30, 2012

    OSS AVL TIBIAL LOCK RING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 14, 2026

    PT2 MODERATE SUPPORT GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC SCIMED, INC.·Product code LOX·June 19, 2006

    ARCHITECT C4000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·February 5, 2024

    CORAIL AMT NECK SEG 135D KHO

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LXH·May 14, 2025

    SPECTRANETICS ELCA LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code LPC·August 8, 2013

    ARCHITECT C16000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·June 30, 2021

    NEUWAVE PR XT PROBE 20CM 15GA

    FDA Adverse Event
    Injury ·NEUWAVE MEDICAL, INC.·Product code NEY·December 20, 2021

    SEG HINGE POST, SZ F 14MM 3DEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·February 21, 2022

    STEM COLLAR 35 MM O.D.

    FDA Adverse Event
    Injury ·ZIMMER TMT·Product code JWH·August 16, 2018

    DEPUY SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC.·Product code KWS·December 6, 2017