BEUDAMED
    33 results · 20ms · Sources: EU EUDAMED, US FDA

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    STRETCH VINYL EXAMINATION GLOVE, POWDER FREE (YELLOW/WHITE/CLEAR(NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Neodent

    FDA UDI
    JJGC Indústria e Comércio de Materiais Dentários S/A.·07899878047315·GM EASYGUIDE SURGICAL KIT CASE REGULAR/WIDE DIA...

    ADVIA Centaur® Multi-Diluent 2

    FDA UDI
    Siemens Healthcare Diagnostics Inc.·00630414175232·Multidil 2 Readypack (2PK) - CENTAUR - CAL - 1x...

    N/A

    FDA UDI
    Smith & Nephew, Inc.·03596010034915·HIBBS OSTEOTOME STRAIGHT 15.8MM

    Humelock II Cemented Shoulder System

    FDA UDI
    FX SOLUTIONS·03701037301180·HUMELOCK II STEM TA6V SIZE 14 CEMENTED

    5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/65MM

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code JDP·August 28, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 26, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·March 2, 2015

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100140·Implant Tray, Cosmolock, Arcamed

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345024090·Paddle Shaver, 14mm

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0103140·Shaver, Closed, 14mm

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K1100140·Implant Tray

    IMPLANT, FIXATION DEVICE CONDYLAR PLATE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code JDP·February 23, 2017

    RAGNELL SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896020412·RAGNELL SCISSORS UNDERMINING SPATULATED CURVED ...

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306815911·Middeldorpf Retractor, 17mm Blade, 20cm

    Aurora Spine

    FDA UDI
    AURORA SPINE, INC.·B5211103140·MALLET, POSTERIOR AND ANTERIOR DISK PREP

    DIMENSION CTNI CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IMNS MEDACTA NAVIGATION SYSTEM,33.221000US

    FDA 510(k)
    FDA Class 2 ·Neurology

    ADVANIX BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 8, 2025

    ADVANIX BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 5, 2024