BEUDAMED
    7 results · 19ms · 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.
    Filters Regulation: Us FDA ×

    STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR

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

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981717·anteriors; shade D3; mould US4

    TRICOS A RESORBABLE BONE SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Life Spine Laminoplasty System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 27, 2013

    ECHELON*FLEX60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·February 8, 2011

    SUPER SUCKER SHORT (BX/20)

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code KDC·December 18, 2013