BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    EXELINT SecureTouch Safety Hypodermic Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Simpact Tri-Fin

    FDA UDI
    Life Spine, Inc.·00190837063153·Sleeve Drill

    SORING GMBH SONOCA LIPO

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AUGMENT AND SCREW, PSA TYPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 7, 2013

    7700

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

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·February 2, 2017

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DYB·May 4, 2018

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·December 16, 2019