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

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    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345027237·Inserter, 7-10MM, Lumbar Straight

    BALLOON CANNULA, SHORT, MODEL R65-985; BALLOON CANNULA, LONG, MODEL R65-985-1

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CovaWound™ Foam 5x10

    FDA UDI
    Covalon Technologies Ltd·00825439011621·Non-Adherent Foam Dressing with Adhesive Border

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964150562·Endo Carry-on Procedure Kit contains Basin, Spo...

    Breathe Easy XL Internal Nasal Splint

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501020812·Breathe Easy XL Internal Nasal Splint, Silicone

    Strub Medical GmbH & Co. KG

    FDA registration
    Strub Medical GmbH & Co. KG·18 products·🇩🇪 Germany

    STRIP-N-TAPE

    FDA UDI
    Conmed Corporation·10653405014225·STRIP-N-TAPE, ADHESIVE TAPE STRIP

    ART-M1, MODEL M1-1-ART-A1

    FDA 510(k)
    FDA Class 2 ·Dental

    OS-2000 OPTICAL SONOGRAPHY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·September 16, 2010

    FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·September 16, 2010

    SYNCHRON® AMYLASE (AMY) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JFJ·September 21, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·March 14, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·June 18, 2010

    FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·September 16, 2010

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 9, 2010

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 14, 2013

    ZIMMER LOCKING ONE-THIRD TUBULAR PLATE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HRS·March 1, 2011

    PACESETTER, INC.

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code DXY·February 15, 2008

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC·Product code GWF·September 27, 2017