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

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    Care Orchestrator Essence

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814299·GENUMEDI PT SILVER R VI

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304438156·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A183226150·18mm H x 32mm W x 26mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A183226120·18mm H x 32mm W x 26mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A18322680·18mm H x 32mm W x 26mm L x 8 degrees ALIF

    SMITH & NEPHEW PEEK INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STERILIZATION MATS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    8CM ANGLE ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 17, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 21, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 28, 2011

    BIOMET CC I-BEAM TIBIAL TRAY 67MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    VANGUARD POSTERIOR STABILIZED TIBIAL BEARING 10X63/67

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    UNKNOWN BIOMET ARCOM 3-PEG PATELLA 31MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·December 19, 2022