BEUDAMED
    8 results · 22ms · 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 ×

    Steriking LT-Blueline Pouches with Tyvek

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PNEUTON MINI VENTILATOR PNEUTON MINI NON-INVASIVE VENTILATION (NIV) KIT ACCESSORY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SCS CLARIS SPINAL SYSTEM, LENGTHENED LATERAL CONNECTOR, MODEL AL06

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELITE 14CM STRAIGHT ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HBE·October 29, 2018

    RAPIDSTRAND

    FDA Adverse Event
    Malfunction ·ANAZAO HEALTH CORPORATION·Product code KXK·July 22, 2011

    ABSORB BIORESORBABLE VASCULAR SCAFFOLD SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·November 3, 2014

    BIG WHL STRTCHR, PRIME X,PWRD

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·July 11, 2013

    GALILEO ECHO V2.0

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·October 18, 2023