BEUDAMED
    88 results · 24ms · Sources: EU EUDAMED, US FDA

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    SPIRODOC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Neodent

    FDA UDI
    JJGC Indústria e Comércio de Materiais Dentários S/A.·07899878047001·NGS REGULAR TAPERED DRILL

    RingLoc® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00880304185630·

    Polyflux

    FDA UDI
    Gambro Dialysatoren GmbH·07332414037925·The Polyflux 140H is intended for use in hemodi...

    Forceps, Micro, round-handle 21.0cm tip 0.4mm

    FDA UDI
    Geister Medizintechnik GmbH·04057034025680·Forceps, Micro, round-handle 21.0cm...

    Uniblate

    FDA UDI
    NAVILYST MEDICAL, INC.·H7877001035301·RITA UniBlate Electrosurgical Device

    MCCOY'S 5A MEDIUM NO. 210-3530

    FDA 510(k)
    FDA Class 1 ·Hematology

    Cortium Universal OCT Spinal Fixation System

    FDA UDI
    Ulrich Medical Usa, Inc.·00814386026437·Screw, Ø 3.5mm, length 30mm, high angulation

    XELIS 3D

    FDA 510(k)
    FDA Class 2 ·Radiology

    EVOLUTION DUODENAL STENT SYSTEM, MODEL EVO-22-27-6-D, EVO-22-27-9-D, EVP-22-27-12-D

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

    ARCOMXL 32MM RLC LNR MROM SZ23

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·June 18, 2018

    CER BIOLOXD OPTION HD 32MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·June 18, 2018

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·August 9, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    MAGNUM HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 8, 2018

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018

    E-POLY LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018