BEUDAMED
    27 results · 22ms · Sources: EU EUDAMED, US FDA

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    KSEA BIPOLAR COAGULATING ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    Preat Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092180860·Biomet 3i Certain®-compatible - 3.4mm Engaging ...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092127575·Biomet 3i Certain®-compatible - 3.4mm Engaging ...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001630·artVeneer life upper anteriors, BXL, BL4

    ActivHeal

    FDA UDI
    ADVANCED MEDICAL SOLUTIONS LIMITED·15032749001637·PHMB Foam Antimicrobial Non-Border, Non-Adhesiv...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092127582·Biomet 3i Certain®-compatible - 3.4mm Engaging ...

    Cervical Plate

    FDA UDI
    Eisertech, LLC·B5231001630·Fixed Awl

    Scanlan® SURG-I-BAND® color coding

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159001273·Scanlan® SURG-I-BAND® color coding - Narrow, Re...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008569·PedFuse Respond, CNL, 8.0mm x 30mm

    MODELS PRIAM (FAMILY OF DEVICES) DIGITAL IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    GORE HYBRID VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·March 7, 2013

    TRUFILL DCS ORBIT MINI COMPLEX FILL

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code HCG·February 25, 2011

    PRECISION XTRA/OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·February 7, 2008