BEUDAMED
    9 results · 22ms · 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 ×

    VARIAX 2 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257129456·20-30 MV FOR MEN CLSC EW STD NAVY VI

    SKINNER TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023741·SKINNER TISSUE FORCEPS WITH TUNGSTEN CARBIDE SE...

    EVERON CENTRAL DISPLAY STATION - CDS, MODEL VERSION 1.0.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SECTRA IDS5 RADIOLOGY WORKSTATION; SECTRA MPR PACKAGE; SECTRA 3D PACKAGE

    FDA 510(k)
    FDA Class 2 ·Radiology

    FREESTYLE PRECISION NEO

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·January 10, 2017

    IDENTITY ADX DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

    IN TOUCH EU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 31, 2013

    UNIVERSAL HIGH TORQUE DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·June 17, 2011