BEUDAMED
    10 results · 32ms · 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.

    MYOEXORCISER II FUAL

    FDA 510(k)
    FDA Class 2 ·Neurology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122376·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 230mm

    TRICAT RIA (ADRENALIN/NORADRENALIN/DOPAMINE); KATCOMBI RIA (ADRENALIN/NORADRENALIN); NORADRENALIN RIA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Hospira Extension Sets

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GLENOSPHERE CENTRIC 36 MM DIAMETER +0 MM LATERAL OFFSET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·December 6, 2021

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    PRECISION XTRA

    FDA Adverse Event
    Injury ·ABBOTT·Product code NBW·January 3, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·July 23, 2014

    36MM VIT E LINER +0MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·December 6, 2021

    Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1. Allura Xper FD10, Model Number: 722010. 2. Allura Xper FD10/10, Model Number: 722011. 3. Allura Xper FD20, Model Number: 722012. 4. Allura Xper FD20 Biplane, Model Number: 722013. 5. Allura Xper FD10 OR Table, Model Number: 722022. 6. Allura Xper FD20 OR Table, Model Number: 722023. 7. Allura Xper FD20 Biplane OR Table, Model Number: 722025.

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·December 18, 2024