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

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    SMART-WELL EZTEST INCUBATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122186·KWire .035x6" (0.9x150mm)

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122179·KWire .035x6" (0.9x150mm) Threaded

    SEEDNET, MODEL FP6T5, FP5T5, FP5T3

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

    OPTICAL TRACKING SYSTEM (OTS)

    FDA 510(k)
    FDA Class 2 ·Neurology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 3, 2013

    SYS 6 RECIP

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·September 16, 2014

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code GAM·May 18, 2011

    VANGUARD INTERLOK FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·May 18, 2018

    VANGUARD INTERLOK XP TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·May 18, 2018

    VANGUARD INTERLOK TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·May 18, 2018

    ARCOM SERIES-A STANDARD PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 18, 2018

    VANGUARD INTERLOK FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·May 18, 2018

    VANGUARD XP LATERAL TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·May 18, 2018