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

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    Filters Regulation: Us FDA ×

    23GA CURVED ILLUMINATING LASER PROBE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SPECTRUM CERVICAL SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SONIXTABLET ULTRASOUND SCANNER

    FDA 510(k)
    FDA Class 2 ·Radiology

    CODA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·October 23, 2017

    BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·September 3, 2024

    INTRACLUDE AORTIC OCCLUSION DEVICE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DXC·May 21, 2013

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 26, 2014

    PALMAZ-SCHATZ BALLOON EXPANDABLE STENT WITH DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code MAF·June 14, 2011

    LOGIC KNEE COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 31, 2024

    CODA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·September 10, 2019

    DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·August 10, 2023