BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    COMBINED MVS SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517379542·CoRoent LO, 16x10x25mm 5°

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111065620·OTIS BOUGIE A BOULE 10FR

    Arch Hook

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746150371·ARCH STOP WELDABLE 2MM 018X025 100/PKG

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·00889981142561·Interbody, 16x14x10mm, 15 Degree, Sterile

    Comet Pressure Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HANS HERMANN LAPAROSCOPES AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·June 5, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·November 29, 2012

    PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·September 28, 2010

    COMP RVRS SHLDR GLNSP STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 28, 2023

    E1 44-36 STD +3 HMRL BRG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 28, 2023