BEUDAMED
    28 results · 27ms · Sources: EU EUDAMED, US FDA

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    BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES AND PREBENT PLATES SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·May 31, 2019

    WALTER LORENZ TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 29, 2017

    BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·June 3, 2016

    N/A

    FDA UDI
    HANS RUDOLPH, INC.·00874750003129·75 V2 SMALL 22ID ELBOW W/HG

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540493651·DRILL F. 12MM SCREWS, STRYKER-SHAFT

    Plateau Spacer System

    FDA UDI
    Life Spine, Inc.·00190837045197·Straight Sizer, 9mm

    Vu a-POD™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981037802·35x27 12mm Spin Plate. The Vu a-POD interverteb...

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376694443·PROXIMITY VA SELF-TAP SCREW, 3.5 x 12mm

    Complete Cervical

    FDA UDI
    Seaspine Orthopedics Corporation·10889981040581·Screw - Self-Tapping - 3.5x12mm

    Segmental Plating System

    FDA UDI
    ALPHATEC SPINE, INC.·00190376545370·SPS VA Self-Tap Screw, 3.5 x 12 mm

    AFFIRM BREAST BIOPSY GUIDANCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MQR·April 12, 2018

    IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 28, 2014

    PRONOVA BLUE MONO POLY(HEXAFLUOROPROPYLENE)SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAW·May 15, 2013

    RESERVOIR 1.8 ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code FRN·May 24, 2011

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MQR·August 17, 2017

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FAD·March 12, 2015

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MQR·March 15, 2018