BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    TDS Standard Solution

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MEP-90 HAIR GROWTH STIMULATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CABLECAP MODEL: WLF, STZ, ACM

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

    SINGLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LJS·December 19, 2017

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code FSA·June 26, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 27, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN-BENNETT CORP.·Product code CBK·September 26, 2008

    VMP ENDURANCE 80G

    FDA Adverse Event
    Malfunction ·DEPUY CMW - 9610921·Product code HTQ·November 27, 2024

    TURBO-FLO SINGLE LUMEN CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·October 1, 2018

    TURBO-FLO SINGLE LUMEN CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·October 1, 2018

    TFNA HELICAL BLADE 90MM STERILE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·March 1, 2024