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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Diode Laser Therapy Device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ACCUTRAY

    FDA UDI
    MEDICAL ACTION INDUSTRIES INC.·10809160290880·

    D-10

    FDA UDI
    BIO-RAD LABORATORIES, INC.·00847817003356·D-10 Hemoglobin A1c Program Calibrator/Diluent Set

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031554·1.6mm x 6mm Stop Contra Angle Drill Bit, Dental...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180149793·SARGIS UTERINE MANIPULATOR TENACULUM

    PEAK MEDICAL

    FDA UDI
    Peak Medical Distribution Inc.·G4533352001180·SARGIS UTERINE MANIPULATOR TENACULUM

    Arena-L®

    FDA UDI
    SPINEFRONTIER, INC.·00190361039273·21X27 TRIAL RASP HEAD, ARENA-L ALLO, 18MM

    GEO 1st MTP Joint Arthrodesis Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HAD1717MC

    FDA 510(k)
    FDA Class 2 ·Radiology

    INSYTE AUTOGUARD IV

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FOZ·December 4, 2001

    Widex

    FDA UDI
    Widex A/S·05706069744392·WIDEX EVOKE EBB3D (Tech Black ) Telecoil, RC co...

    Widex

    FDA UDI
    Widex A/S·05706069882964·WIDEX MOMENT MRB2D (Tech Black ) Telecoil, RIC ...

    NEEDLE 30GA 1/2IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·January 5, 2021

    MULTI-DAY INFUSOR

    FDA Adverse Event
    Malfunction ·IRVINE·Product code MEB·March 28, 2001

    LEVEEN NEEDLE ELECTRODE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEI·October 15, 2008

    ADVIA CENTAUR XP PROSTATE-SPECIFIC ANTIGEN (PSA) ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MTF·August 10, 2011

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 1, 2013

    HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·September 11, 2020

    SMR CEMENTLESS MINI STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code HSD·January 21, 2020

    ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 30, 2019