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

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    WILLI GELLER CREATION AND LF PORCELAIN

    FDA 510(k)
    FDA Class 2 ·Dental

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040044889·Curette Gracey DE 5/6

    Bard® Parsonnet Pulse Generator Pouches

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741040955·Bard® Parsonne Pulse Generator Pouch, Small

    NGB-022 Needle-guided Bracket

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904051475·

    PENADAPT 10

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

    ARTHROCARE FLOW CONTROL UNIT

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

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    SYNCHRO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 9, 2009

    SYNCHRO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 9, 2009

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

    SYNCHRO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code DQX·September 4, 2009

    SYNCHRO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code DQX·September 4, 2009

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006