BEUDAMED
    9 results · 36ms · Sources: EU EUDAMED, US FDA

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    SPIRAL SCALP ELECTRODE, 14499A

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NON-BR2000 LARGE BONE BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919095385·KM71-553

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X180MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 1, 2012

    W&H Assistina Twin

    FDA 510(k)
    FDA Class 1 ·Dental

    ENDOSCOPIC PLICATION SYSTEM; EPS; PLICATOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWP·April 24, 2014

    ALLERGAN

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 27, 2012

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 27, 2010

    NAMIC Convenience Kit, 3 VALVE KIT CARDIOVASCULAR PROCEDURE KIT, UPN H749600403131, REF/Catalog No. 60040313, STERILE, Rx ONLY --- --- For single use only. --- Device Listing Number D136588. Product Usage: NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.

    FDA Enforcement
    Class II ·Terminated·Navilyst Medical, Inc·March 4, 2015