BEUDAMED
    57 results · 21ms · Sources: EU EUDAMED, US FDA

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    AMSURE 3-WAY HYDROPHILIC LATEX FOLEY CATHETER

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

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964069017·Endo Carry-On Procedure Kit

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756032636·Cellulose Burn Pad 23PLY

    NAMBUCCA Anterior Lumbar Plate Screw

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215019990·

    MECHANICAL WHEELCHAIR, MODEL DS 202-S

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    AGILENT M2636B TELEMON B MONITOR (TELEMON B)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    Widex

    FDA UDI
    Widex A/S·05706069722758·Widex CLEAR330 C3-FS BTE (Cappuccino brown S-33...

    Widex

    FDA UDI
    Widex A/S·05706069720815·Widex UNIQUE U-PA BTE (Cappuccino brown S-330 )...

    Widex

    FDA UDI
    Widex A/S·05706069721904·Widex D-FS BTE (Cappuccino brown S-330 ) Teleco...

    Widex

    FDA UDI
    Widex A/S·05706069726909·Widex EVOKE E-PA (Cappuccino brown S-330 ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069721584·Widex UNIQUE U-FS BTE (Cappuccino brown S-330 )...

    Widex

    FDA UDI
    Widex A/S·05706069721096·Widex BEYOND B-F2 (Cappuccino brown S-330 ) Tel...

    Widex

    FDA UDI
    Widex A/S·05706069722321·Widex D-PA BTE (Cappuccino brown S-330 ) RC coil

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

    KYPHOPAK TRAY

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·November 6, 2019