BEUDAMED
    12 results · 20ms · 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 ×

    BONOS INJECT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036029685·

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776364120·Oral Upper Molar Forcep,

    URINE AMPHETAMINE/METHAMPHETAMINE (AMPH) SCREEN FLEX REAGENT, CATALOG NO. DF 90A

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LIFELINES TRACKIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    M2A-T M/H RAD 2HL SHL 41/58MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 12, 2017

    32MM M2A MOD HEAD +3MM NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·October 12, 2017

    M2A-TAPER LINER SZ 41/32

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 12, 2017

    CD HORIZON

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·September 21, 2015

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·May 2, 2013

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code MNT·September 15, 2014

    MONOPOLAR CURVED SCISSORS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·October 4, 2013