BEUDAMED
    11 results · 21ms · 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 ×

    TCS Blend

    FDA 510(k)
    FDA Class 2 ·Dental

    Equator

    FDA UDI
    Preat Corporation·00842092176641·Equator Abutment for Astra EV 3.0 x 4mm

    CLASSIX CHEMICAL STERILIZATION INDICATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IMALUX NIRIS IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    RADIUS-7

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·July 2, 2015

    RESTYLANE L, RESTYLANE LIDOCAINE

    FDA Adverse Event
    Injury ·Q- MED·Product code LMH·May 29, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 12, 2014

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWP·June 22, 2011

    PATIENT SAFETY NET

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code MSX·March 31, 2016

    PATIENT SAFETY NET

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code MSX·March 31, 2016

    APEX HOLE ELIM POSITIVE STOP

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 24, 2020