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

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    Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PHYSIOLOGICAL DATA PROCESSOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Fix2Lock (PEEK Self Punching)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CRYO CATHETER FREEZOR XTRA 3

    FDA Adverse Event
    Malfunction ·CRYOCATH TECHNOLOGIES INC·Product code NFC·October 26, 2008

    SEPRAFILM (SODIUM HYALURONATE, CARBOXYMETHYLCELLULOSE) MEMBRANE

    FDA Adverse Event
    GENZYME BIOSURGERY (SEPRAFILM/PACK)·Product code MCN·August 2, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 12, 2013

    BD KIESTRA IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025

    BD KIESTRA¿ IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·December 9, 2024

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025