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

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    ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103

    FDA 510(k)
    FDA Unclassified ·Unknown

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981212858·Trial 9w, 9mm

    XIPHOS ZFUZE

    FDA UDI
    Difusion Technologies, Inc.·00853896008151·PLIF Spacer 29mm Long x 9mm Height

    PLAINSENSE WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    HP M2376A DEVICE LINK SYSTEM, MODEL M2376A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    NA

    FDA UDI
    Zimmer, Inc.·00889024065451·

    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