BEUDAMED
    11 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.

    ARMSTRONG V VENT TUBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Tranquil-C™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788223750·Cervical Rasp + DS 12x12x12 Flat

    BABY CHICK BLOOD IN ALSEVER'S

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AMPCO SKIN SCRUB TRAY

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·July 29, 2021

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 20, 2014

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·September 1, 2010

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 8, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·April 6, 2018

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 19, 2019