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

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    NC-STAT

    FDA 510(k)
    FDA Class 2 ·Neurology

    Zavation

    FDA UDI
    Zavation LLC·00842166120846·Spinous Process Plate Assembly 35mmx8mm

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065845·EXTRAORAL ELASTICS 3/8" 8 oz

    GEN4 Direct Access

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828101967·GEN4 Direct Access

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·ECWG0035081·CC/ Transition Dentine TD-B3

    LIFEPAK® 12 defibrillator/monitor

    FDA UDI
    PHYSIO-CONTROL, INC.·00885074857770·LP12AABAABAACABBAABAAAAALP12 MONITOR-DEFIB

    NorthStar

    FDA UDI
    Seaspine Orthopedics Corporation·10889981195922·Poly. Screw, 3.5mm x 8mm

    LASERSKIN DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    THERMOFLEX SYSTEM

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

    NA

    FDA UDI
    STRYKER CORPORATION·04546540046659·Thin Offset (13.0 x 0.38 x 39.0mm)

    Spacelabs Healthcare

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522124938·4 ELECTRODE EVO RECORDER BELT MOUNTED, BR PORTUG

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·July 21, 2016

    JAW INS.BIP.MACRO FORCEPS D: 5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG TUTTLINGEN 78532·Product code GEI·December 12, 2014

    BIPOLAR MACRO FORCEPS D:5/ 310MM

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

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·January 14, 2015

    Gibralt

    FDA UDI
    Choice Spine, LP·10885862006738·

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 6, 2025

    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