BEUDAMED
    29 results · 23ms · Sources: EU EUDAMED, US FDA

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    SIEMENS-ELECTROGERATE GMBH MICRO-INHALER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Sphero Attachment

    FDA UDI
    Preat Corporation·00842092118627·Sphero Block Abutment 3i Osseotite 3.5mm x 0mm ...

    Polishers

    FDA UDI
    DFS - DIAMON GmbH·04057176152343·2comp polisher lense RA

    HEART STABILIZER FINGER ATTACHMENT

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09928008300·HEARTLINE HEART STABILIZER FINGER ATTACHMENT 2S...

    HEART STABILIZER FINGER ATTACHMENT

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896070318·HEARTLINE HEART STABILIZER FINGER ATTACHMENT 2S...

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016250135·Ultima System PFX - 230V UPS

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016250104·Ultima System PFX

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·B368800830011·Ultima System PFX - 120V UPS

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016250128·Ultima System PFX

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·B368800830001·Ultima System PFX

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016250111·Ultima System PFX - 120V UPS

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·B3688008300210·Ultima System PFX

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·B3688008300310·Ultima System PFX - 230V UPS

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867042551·4 HOLE DBL COMP PLT,STR,30MM

    CANNULATION TOURNIQUET SET, 2 TUBE OR 5 TUBE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M7/M7T DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    11.0MM TI HELICAL BLADE 115MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HSB·August 22, 2017

    COMPLETE SE ILIAC

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIO·October 23, 2012

    GALILEO ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·May 8, 2014