BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    NUVO IF Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    SBH

    FDA UDI
    SBH Surgical·00850068304011·1/1, Sterilization Container Perforated Lid, Bl...

    INTEGRATED REGISTRATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    GC AADVA BO AC ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    RATE FLOW REGULATOR IV SET

    FDA Adverse Event
    Other ·B. BRAUN MEDICAL, INC.·Product code FPA·October 6, 2008

    HT70 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·June 25, 2013

    TENDRIL ST

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·August 5, 2011

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 21, 2011

    WarmAir 135 Thermal Regulating System. Catalog Numbers: 86186-115 V, 06186-115 V (sold in the U.S.) and #86185-100 V ( not sold in the U.S.). Intended for warming patients before, during and after surgery, and other specialty procedures.

    FDA Recall
    Terminated ·Cincinnati Sub-Zero Products Inc·Product code DWJ·February 16, 2009