BEUDAMED
    41 results · 21ms · Sources: EU EUDAMED, US FDA

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    APNOESCREEN PRO, ALPHA SCREEN PRO

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741096150·Catheter Placement Kit

    SoftTip® large

    FDA UDI
    Honeywell Healthcare Solutions GmbH·04036616005678·SoftTip® large R-2414-30 HP/Philips

    MEDALLION MODULAR HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304639898·

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057374784·Skytron Stirrup Clamp

    NA

    FDA UDI
    David Scott Company·15060797554058·Stirrup Clamp, Blade Style, attaches anywhere o...

    TUFF TT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·September 11, 2024

    Eclipse Pro

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522129735·ECLIPSE PRO,DEFIB CABLE,PX,10 SNAP,IEC

    Eclipse Pro

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522131400·ECLIPSE PRO,DEFIB CABLE,PX,10 SNAP,IEC,UKCA

    DC BEAD

    FDA Adverse Event
    Injury ·BIOCOMPATIBLES UK LTD·Product code KRD·March 27, 2018

    DC BEAD

    FDA Adverse Event
    Injury ·BIOCOMPATIBLES UK LTD·Product code KRD·March 27, 2018

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00850043222354·Skytron Stirrup Clamp (JPN)

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057374791·Skytron Stirrup Clamp (EU)

    ACCESS MYOGLOBIN ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33310, 33315, 33319, 33316

    FDA 510(k)
    FDA Class 2 ·Immunology

    ONTRAK TESTSTIK FOR METHAMPHETAMINE, CAT. 1986686

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    BIOMET MICROFIXATION FACIAL PLATING SYSTEM

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code JEY·August 17, 2021

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·March 12, 2013

    COMPLETE SE PERIPHERAL STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code NIO·February 18, 2011

    PFC KEEL TIB TRAY CEM SZ3

    FDA Adverse Event
    Injury ·DEPUY - RAYNHAM A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 19, 2008

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FGB·August 29, 2024