BEUDAMED
    36 results · 27ms · Sources: EU EUDAMED, US FDA

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    NYLON NONABSORBABLE SURGICAL SUTURES, USP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964004702·CUSTOM PROCEDURE KIT

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741105197·Catheter Placement Kit

    Sledgehammer

    FDA UDI
    Keystone Industries·H66810005391·SC 1 lb Pwd & 8 oz Liq Kit, Lt Fibered

    GeneXpert Infinity-48s System

    FDA UDI
    CEPHEID·07332940004323·

    K090539

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·February 26, 2026

    INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MIDAS TOUCH BLUE NITRILE EXAMINATION GLOVES-POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·May 1, 2023

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADVANCED

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    DREAMSTATION BIPAP AUTOSV

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code MNS·January 16, 2023

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADV SYSTEM ONE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 21, 2022

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 12, 2026

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code MNS·October 31, 2022

    ILAB ULTRASOUND IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (CE)·Product code OBJ·March 12, 2013

    CLEARTRACE ADULT ECG ELECTRODE

    FDA Adverse Event
    CONMED CORPORATION·Product code DRX·February 24, 2011

    ELECSYS 2010 RACK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS CORP.·Product code JJE·February 15, 2008