BEUDAMED
    19 results · 26ms · Sources: EU EUDAMED, US FDA

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    Diamondback 360 Peripheral Orbital Atherectomy System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Leg Bag

    FDA UDI
    C. R. Bard, Inc.·00801741050862·Dispoz-A-Bag, Leg Bag with Flip-Flo Drainage Va...

    HHM

    FDA UDI
    Oticon A/S·05707131281098·H160V2, MINIBTE 312 WL 85 SGR HHM

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100110·FEASTER SPECULUM SOLID WIDE

    EMULSION SB

    FDA 510(k)
    FDA Unclassified ·Unknown

    FORA G30A BLOOD GLUCOSE MONITORING SYSTEM, MODEL TD-4241

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    URINE COLLECTION DRAIN BAG

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·May 25, 2022

    LATEX FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·May 25, 2022

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·January 7, 2016

    DISPOZ-A-BAG, LEG BAG WITH FLIP-FLO DRAINAGE VALVE

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code FAQ·April 8, 2026

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    UNKNOWN IMPLANTABLE PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 6, 2013

    ARCHITECT HAVAB-M

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code LOL·July 6, 2011

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·September 3, 2008

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·May 24, 2016

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021