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

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    PRESSUREWIRE AERIS AGILE TIP; PRESSUREWIRE AERIS AGILE TIP 300

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SILVERSEAL

    FDA 510(k)
    FDA Unclassified ·Unknown

    DISPOSABLE BLLOD COLLECTION NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 20, 2013

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 19, 2008

    EON RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL- NEUROMODULATION·Product code LGW·June 16, 2011

    G7 OSSEOTI 4 HOLE SHELL 54MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 14, 2025

    G7 LONGEVITY NEUTRAL 36MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 14, 2025

    CLS® SPOTORNO®, STEM, 135°, UNCEMENTED, 9.0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·January 30, 2025

    Achieva 1.5T

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·November 29, 2023