BEUDAMED
    301 results · 21ms · Sources: EU EUDAMED, US FDA

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    Dunamis Interference Screw

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169502185·INTERBODY 2151220 MEDIUM - 6 DEG 20MM

    FLEXTEND IS-1 BI POSITIVE FIX

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code DTB·May 7, 2004

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192312·Revision Knee Reamer Spiral Fluted - Zimmer 22mm

    TALOS®-A

    FDA UDI
    SpineArt SA·07640375238009·TALOS®-A (HA) PEEK PLANAR, SYMMETRIC IBFD D28 ...

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321512200·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311512200·

    Flextrode

    FDA UDI
    COSMAN MEDICAL, LLC·08132500133826·Electrode 15cm, 13mm Tip, 20G

    NA

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·00813250013382·Flextrode, 15cm,17G Introducer

    CHIC

    FDA UDI
    Gc Orthodontics America Inc.·D78815122000201·CHIC MINI MBT 018/UL2 10T 8A

    CHIC

    FDA UDI
    Gc Orthodontics America Inc.·D78815122000101·CHIC MINI ROTH 018 UL2 8T 9A 0OF

    EXPLORER 4D TREATMENT PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    REPROCESSED DEFLECTABLE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 8, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    UNKNOWN DEPUY ULTAMET 54X36 LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·June 30, 2011

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 9, 2022

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026