BEUDAMED
    62 results · 24ms · Sources: EU EUDAMED, US FDA

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    JET THERAPY

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981212841·Trial 9w, 8mm

    Metal Custom Rx

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746105166·BRACKET V-SLOT SINGLE WIDTH MAND LEFT CUSPID 01...

    XIPHOS ZFUZE

    FDA UDI
    Difusion Technologies, Inc.·00853896008144·PLIF Spacer 29mm Long x 8mm Height

    SKYLIGHT IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    KONTUR 55 SOFT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    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