BEUDAMED
    34 results · 22ms · Sources: EU EUDAMED, US FDA

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    Pressure Therapy System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Oticon

    FDA UDI
    Oticon A/S·05707131305343·SENSEI PRO, BTE 312 WL 75 PUW

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528104071·ExtremiFix Large, 6.5 mm Headless Screw Module

    HAcancellous™ PEEK-C

    FDA UDI
    INNO Holdings, Inc.·M711591619070·HAcancellous PEEK-C, 16L x 19W x 7H x 8°, HA PE...

    Cadet Cervical Cage

    FDA UDI
    VALORUS SPINE LLC·00811771034367·Cadet Cervical Cage, 16mm x 19mm x 07mm, 7° Lor...

    Cadet Cervical Cage

    FDA UDI
    VALORUS SPINE LLC·00811771033735·Cadet Cervical Cage, 16mm x 19mm x 07mm, Non-Lo...

    HAEMONETICS CELL SAVER ELITE AUTOTRANSFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MODIFICATION TO: DATEX-OHMEDA S/5 ENTROPY MODULE, E-ENTROPY AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Neurology

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 10, 2014

    CONSULTA CRT-P

    FDA Adverse Event
    Death ·IPG MFG SWITZERLAND·Product code NVZ·June 11, 2013

    ARTICULEZE M HEAD 36MM-2

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·July 11, 2011

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·February 20, 2020

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·February 28, 2020

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·February 28, 2020