BEUDAMED
    10 results · 36ms · 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.

    ALKO FLUIDS PACKS FOR NOVA ANALYZERS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CLARITY LPC LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GE MOBILE DISCOVERY ST PET CT IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEGA SUTURECUT NEEDLE DRIVER

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 25, 2013

    SPIN SCREW DIAM. 2MM LG 14MM

    FDA Adverse Event
    Malfunction ·NEWDEAL S.A.S.·Product code HWC·November 18, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 11, 2014

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 5, 2015

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 9, 2015

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 30, 2018