BEUDAMED
    10,000 results · 37ms · 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 ×

    PHOENIX

    FDA Adverse Event
    Other ·GAMBRO DASCO·Product code FII·July 21, 2006

    KGS BIOMET CC CRUCIATE TRAY 71MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·December 23, 2025

    ALARIS SMART PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·August 13, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 10, 2017

    BM11A BLOOD MONITOR PUMP (REFURBISHED)

    FDA Adverse Event
    Malfunction ·MESYS·Product code FKP·September 5, 2002

    SWIVEL ARM FOR 25 KGS. VAE/VAG

    FDA Adverse Event
    Malfunction ·BERCHTOLD GMBH & CO. KG·Product code FSY·March 24, 2016

    HICKMAN S/L CATHETERS

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJS·April 18, 2019

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code KDI·October 24, 2003

    UNK ATTUNE KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·March 31, 2025

    MERIDIAN FILTER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 25, 2019

    UNK ATTUNE KNEE PATELLA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 1, 2025

    UNK ATTUNE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 1, 2025

    UNK ATTUNE KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·March 31, 2025

    UNK ATTUNE KNEE PATELLA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·March 31, 2025

    UNK ATTUNE KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·March 31, 2025

    UNK ATTUNE KNEE PATELLA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·March 31, 2025

    UNK ATTUNE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·March 31, 2025

    BARD MAXCORE DISPOSABLE BIOPSY INSTRUMENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 4, 2019

    S/L PERC 8FR 65D

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJS·July 24, 2019

    INCUBATOR

    FDA Adverse Event
    DRAGERWERK AG·Product code FMZ·March 22, 1996