BEUDAMED
    14 results · 19ms · Sources: EU EUDAMED, US FDA

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    BRANNON PEDI PORTSYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295232285·P.F.C. SIGMA FEMORAL CRUCIATE SUBSTITUTING CEME...

    Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 2 ·OSTEONICS CONSTRAINED ACETABULAR INSERT

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556864241·HUMERAL REAMER MOD

    CARTO RMT EP NAVIGATION SYSTEM V8

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRAY, BLADDER IRRIGATION

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

    FDA Pre-Market Approval
    HOWMEDICA OSTEONICS CONSTRAINED ACETABULAR INSERT & TRIDENT CONSTRAINED ACETABULAR INSERT

    FDA Pre-Market Approval
    OSTEONICS CONSTRAINED ACETABULAR INSERT

    FDA Pre-Market Approval
    OSTEONICS CONSTRAINED ACETABULAR INSERT

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780247265·Titan™ Reverse Shoulder System Humeral Reamer T...

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 29, 2014

    MICRO OSCILLATING SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·December 6, 2010

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·AQUATEC OPERATIONS GMBH·Product code FSA·February 13, 2013

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017