BEUDAMED
    38 results · 67ms · 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.

    MODIFICATION TO CARTO EP NAVIGATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810001901·REAMERS 21MM

    DTS-3000

    FDA UDI
    DAESUNG MAREF CO.,LTD.·08809315676519·BLUE MAIN HOSE 1ea

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040093570·Maxima Reamers 21mm

    ISOLA

    FDA UDI
    DEPUY SPINE, LLC·10705034005676·ISOLA SPINE SYSTEM OPEN HOOK 4.75 x 5.0mm

    intellijoint HIP®

    FDA UDI
    Intellijoint Surgical Inc·00628184001905·Screw, Femur, G2

    eWave 6-Lead EKG

    FDA UDI
    Wearlinq, Inc.·K00010·Continuous wearable electrocardiogram (ECG) mon...

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2520001900·Curved Ti Rod, 190mm

    DuoFLEX® Coil Suite

    FDA UDI
    M R Instruments, Inc.·00857371006168·The 24cm Left Coil Assembly is a part of the Du...

    DuoFLEX® Coil Suite

    FDA UDI
    M R Instruments, Inc.·00857371006175·The 24cm Right Coil Assembly is a part of the D...

    FlowLogic Agile

    FDA UDI
    SONENDO, INC.·00810209420925·FlowLogic Agile Shaping File .04 Kit, 21mm

    CAMLOG ROOTFORM IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SMR GLENOSPHERE Ø36 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·August 26, 2021

    SMR SHOULDER

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 3, 2024

    UNKNOWN INTELLIJOINT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 12, 2013

    INFUSOR TWO DAY 2ML/HR 12 PK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 24, 2011

    TRIDENT CERAMIC LINER

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MRA·February 19, 2008

    FEMORAL MODULAR HEAD - M Ø36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·September 8, 2021