BEUDAMED
    10 results · 23ms · 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 ×

    Medtronic Transportation/Sterilization Cassettes

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Geneva

    FDA UDI
    Nucletron B.V.·08717213056251·Interstitial Ovoid 40mm 2

    Acetabular Reamer 41 mm

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215098803·

    DISC-FX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT

    FDA 510(k)
    FDA Class 1 ·Dental

    PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·October 3, 2014

    MAXIMO VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 7, 2013

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2011

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023