BEUDAMED
    1,290 results · 102ms · 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 ×

    EXACT MEDICAL MANUFACTURING, INC.

    FDA Adverse Event
    Malfunction ·EXACT MEDICAL MANUFACTURING, INC.·Product code KKX·December 23, 2024

    NA

    FDA Adverse Event
    Injury ·EXACT MEDICAL MANUFACTURING INC.·Product code FYA·May 31, 2013

    HALYARD VIDEO DRAPE 5IN - 96IN

    FDA Adverse Event
    Injury ·O&M HALYARD, INC.·Product code KKX·June 18, 2024

    SHOCKWAVE M5+ PERIPHERAL INTRAVASCULAR LITHOTRIPSY (IVL) CATHETER

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code PPN·March 27, 2025

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·March 9, 2021

    Q2 MULTIPORT MANIFOLD IV ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code FPA·April 23, 2013

    INTROCAN SAFETY

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·July 25, 2013

    ARM & HAMMER SPINBRUSH SONIC BATTERY UNSPECIFIED

    FDA Adverse Event
    Malfunction ·CHURCH & DWIGHT CO., INC.·Product code JEQ·August 29, 2019

    LACRICATH LACRIMAL DUCT CATHETERS

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code OKS·November 11, 2014

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·December 7, 2023

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·December 7, 2023

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code FPD·February 18, 2021

    VRVII - CLEAR

    FDA Adverse Event
    Injury ·QUEST MEDICAL, INC.·Product code DWD·June 7, 2015

    VRVII - CLEAR

    FDA Adverse Event
    Injury ·QUEST MEDICAL, INC.·Product code DWD·June 7, 2015

    DREAMSTATION CPAP

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·January 9, 2025

    ON-Q C-BLOC WITH DUAL SELECT-A-FLOW* 600 ML X 1-7 ML/HR + 1-7 ML/HR

    FDA Adverse Event
    Malfunction ·HALYARD - IRVINE·Product code MEB·October 12, 2018

    HEMOLUNG RAS

    FDA Adverse Event
    Injury ·ALUNG TECHNOLOGIES, INC.·Product code DQR·February 27, 2023

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·March 28, 2024

    ALERE DETERMINE HIV 1/2 AG/AB COMBO

    FDA Adverse Event
    Malfunction ·ALERE SCARBOROUGH INC.·Product code MZF·June 13, 2018

    DREAMSTATION CPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·May 30, 2025