BEUDAMED
    12 results · 18ms · 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.

    ECHOMARK CSI INTERFACE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909109652·REVELATION DIAMOND 877K-014M - 5 PACK

    AlphaVent

    FDA UDI
    STRYKER CORPORATION·07613327563160·ALPHAVENT SUTURE ANCHOR 6.5MM PEEK, SUTURE ANCH...

    AlphaVent

    FDA UDI
    STRYKER CORPORATION·07613327563221·ALPHAVENT SUTURE ANCHOR 6.5MM PEEK, SUTURE ANCH...

    AlphaVent

    FDA UDI
    STRYKER CORPORATION·07613327563207·ALPHAVENT SUTURE ANCHOR 6.5MM PEEK, SUTURE ANCH...

    AlphaVent

    FDA UDI
    STRYKER CORPORATION·07613327563238·ALPHAVENT SUTURE ANCHOR 6.5MM PEEK, SUTURE ANCH...

    A-LINE AEP MONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER 36/+6MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·February 17, 2021

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 11, 2013

    PROFEMUR(R) Z STEM PLASMA SPRAYED

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·November 30, 2010

    ATLAS II VR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 2, 2014