BEUDAMED
    22 results · 22ms · Sources: EU EUDAMED, US FDA

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    ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2076-XXYY, 2092-XXYY, 2105-XXYY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bur PM2-70 50K Steel Ø7.0

    FDA UDI
    Bien-Air Surgery SA·07630055502766·

    BoneSync Fast-Setting Drillable Calcium Phosphate Cement

    FDA UDI
    DSM BIOMEDICAL, INC.·00812337029209·Fast-Setting Drillable Calcium Phosphate Cement

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694001908·8mm Pyriform Rigid Plate

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869634441·MOSS VRS Locking Cap Star 27 Tightener, 1/4" co...

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869697620·MOSS VRS MIS Locking Cap final tightener ISR27,...

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869639880·MOSS 100 Counter Torque Sleeve

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694063357·2OS 8mm Pyriform Rigid Plate Sterile Qty 5

    ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEALTHCARE SERVICE AND SUPPLY ALP ALTERNATING LEG PRESSURE PUMP AND GARMENTS FOR THE LIMB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROGAV®

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·January 3, 2018

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code PAH·May 8, 2013

    INFUSOR

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

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·May 15, 2008

    Radio Capitellum Broach Large, Right. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.

    FDA Enforcement
    Class II ·Terminated·Howmedica Osteonics Corp.·August 15, 2018

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 7, 2024

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 3, 2025

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 3, 2025

    DISPOSABLE STERILE HIGH TEMPERATURE ELECTROCAUTERY (HTC) F7244

    FDA Adverse Event
    Injury ·FIAB SPA·Product code GEI·October 12, 2023

    ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100

    FDA Recall
    Terminated ·Life-Tech International, Inc·Product code CAZ·May 9, 2001