BEUDAMED
    7 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.

    REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER

    FDA 510(k)
    FDA Class 1 ·Dental

    SeaSpine Spacer System - Ventura™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981033330·10mm Long Ventura Trial

    ZIMMER TRABECULAR METAL REVERSE SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VITAL SIGNS MONITOR, PROPAQ LT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SECURE 3 MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV·Product code FNL·December 14, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 14, 2014

    ARTICULATING HOOK WITH MONOPOLAR CAUTERY

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL·Product code GCJ·December 21, 2012