BEUDAMED
    46 results · 20ms · Sources: EU EUDAMED, US FDA

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    NAC Y-ADP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040073223·Carbide Bur FG 329

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741038181·Catheter Placement Kit

    ELIMINATOR

    FDA UDI
    Conmed Corporation·20653405052446·CONMED ELIMINATOR 3-Stage Esophageal PET Balloo...

    Brite-Gear

    FDA UDI
    ORMCO CORPORATION·00889989023503·Facebow MINSHORT#3 044 PINK

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167700003430·

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1700003430·

    MIDAS TOUCH NITRILE EXAMINATION GLOVES-POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DRG AURICA ELISA TESTOSTERONE KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CARDIOSAVE HYBRID, TYPE I PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 12, 2026

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·February 13, 2025

    ELIMINATOR PET BALLOON DILATOR

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code KNQ·August 1, 2019

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·March 12, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 18, 2011

    PERICARDIAL TISSUE HEART VALVE

    FDA Adverse Event
    Injury ·EDWARD LIFE SCIENCES·Product code LWR·February 7, 2008

    PADGETT MODEL S SLIMLINE ELECTRIC DERMATOME

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code GFD·March 9, 2018

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 3, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 3, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 3, 2024

    ALINITY M SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code OOI·February 3, 2022