BEUDAMED
    1,145 results · 29ms · Sources: EU EUDAMED, US FDA

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    BNA ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    K121116

    FDA UDI
    Life Spine, Inc.·00190837016029·

    Plateau-X Spacer System

    FDA UDI
    Life Spine, Inc.·00190837016043·

    Plateau-X Spacer System

    FDA UDI
    Life Spine, Inc.·00190837016258·

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780377061·Integra® Jarit® Webster Needle Holder, 4-5/8", ...

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172974032·UniTip High Resolution Catheter 12F

    POWDERED BROWN LATEX SURGICAL GLOVES, STERILE WITH EXPIRATION DATE LABELING CLAIM & PROTEIN CONTENT LABELING CLAIM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SYNGO DOSIMETRIST WORKSPACE V2.7 MODEL: 1056864

    FDA 510(k)
    FDA Class 2 ·Radiology

    Widex

    FDA UDI
    Widex A/S·05706069886108·WIDEX MOMENT MRB0 (Silver Grey ) 220, RIC 10

    Widex

    FDA UDI
    Widex A/S·05706069920345·WIDEX MOMENT MBB3D 220 DEMO (Silver grey)

    Widex

    FDA UDI
    Widex A/S·05706069812350·Widex EVOKE E-PA (Silver Grey ) 220, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069884777·WIDEX MOMENT MRR2D DEMO (Silver Grey ) 220, RC ...

    PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·April 10, 2018

    PEDICLE SCREW 7X50

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 23, 2018

    PEDICLE SCREW 5X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·March 23, 2018

    GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·January 5, 2017

    M.U.S.T. RODS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·April 20, 2026

    PEDICLE SCREW PEDICLE SCREW 5X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·January 17, 2024

    M.U.S.T. POLYAXIAL PEDICLE SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·October 28, 2024

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·May 20, 2013