BEUDAMED
    24 results · 54ms · 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 ×

    LF-DP GASTROINTESTINAL AND SIGMOID FIBERSCOPE, ACCESSORIES AND ANCILLARY EQUIPMENT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    002231

    FDA UDI
    PATHEN MEDICAL LLC·00850005864585·Extension Set, 6" w/ 3-way stopcock

    Procure

    FDA UDI
    Twin Med, LLC·10840330700365·Mask Venturi Adult W/complete set: diluter jets...

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159007916·Baby Vascular Profunda Clamp With Atraumatic Jaw

    TRIAGE BNP CALIBRATION VERIFICATION CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    THE KALIX IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD PLASTIPAK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 23, 2022

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·March 13, 2013

    UNKOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

    PFC SIG RPF CEM FEM SZ RT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC., DIVISION - DEPUY-RAYNHAM·Product code NJL·February 20, 2008

    UNKNOWN NEXGEN FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 17, 2019

    ANEURX ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·April 23, 2012

    TALENT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·April 23, 2012

    METRX SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    ELITE 12CM STRAIGHT ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HBE·January 22, 2021

    1.5MM SYSTEM 2 HOLE LONG STRAIGHT PLATE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·May 1, 2018