BEUDAMED
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    SI-BONE iFuse Implant System®

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HHM

    FDA UDI
    Oticon A/S·05707131342638·G200, MINIRITE T 312 2.4G C091 HHM

    PIVIT A/B ST AND PIVIT A/B ST-R

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

    VOYAGER TRANSPORT INCUBATOR WITH MASIMO PULSEOX, VOYAGER TRANSPORT INCUBATOR WITH NELLCOR PULSEOX

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HUT EXT DR FINAL ASSY-STANDARD

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO·Product code KQS·October 9, 2008

    INSTA TRAK 3500

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code LLZ·July 21, 2011

    CYLOS DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code DXY·June 27, 2013