BEUDAMED
    39 results · 24ms · Sources: EU EUDAMED, US FDA

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    IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artegral life HD

    FDA UDI
    Merz Dental GmbH·D7092004011·artegral life HighDefinition posterior lower -M...

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193105604·HA PEEK EVOS Straight, ,11mmx9mmx 26mm , FLAT ...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540400970·FLUOROSCOPY ADAPT. (PHILIPS BV300,9'')

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF20040110·2.0mm Cortex Screw, 1.5 Hex, Self-Tapping, 11mm

    CHILI VIDEO, CHILI VIDEOPRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFIED HYDROPHILIC COATED GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANATOMICAL SHOULDER SYSTEM METAL HUMERAL HEAD Ø40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWS·October 5, 2022

    MINIMED QUICK-SET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 24, 2024

    QUICK SET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 4, 2025

    QUICK SET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 4, 2025

    HEARTMATE II LVAD

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·March 12, 2013

    CONTASURE

    FDA Adverse Event
    Injury ·NEOMEDIC INTL S.L.·Product code FTL·February 23, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·February 26, 2008

    VERSA-DIAL 46X24X47 HUM HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·April 24, 2013

    200 MICRON TFL BALL TIP SINGLE USE FIBER

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code GEX·February 14, 2024

    PC HYBRID GLENOID POST- POLY

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013

    SM HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013

    2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW 2.7 X 10MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·August 31, 2020

    TMJ SYSTEM CROSS DRIVE FOSSA SCREW 2.0MM X 7MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·August 31, 2020