BEUDAMED
    130 results · 29ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO HI-ART TREATMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Malecot

    FDA UDI
    COOK INCORPORATED·00827002147959·Percutaneous Malecot Nephrostomy Set

    FIBONACCI™ PROXIMAL LATERAL TIBIA PLATE, RIGHT, 5 HOLE

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665035254·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694038805·2.0mm x 5mm Midface Screw

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR76000820051·Lingual cleat on pad max. left / mand. right

    MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BOLUSPRO ULTRA

    FDA 510(k)
    FDA Class 2 ·Radiology

    SGARLATO LABS

    FDA Adverse Event
    Malfunction ·SGARLATO LABS·Product code JDW·March 30, 2007

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC, INC., NEUROLOGICAL DIVISION·Product code LKK·August 22, 2005

    SYNCHROMED II

    FDA Adverse Event
    Other ·NEUROLOGICAL DIVISION, MEDTRONIC, INC.·Product code LKK·September 29, 2005

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·April 3, 2006

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·September 22, 2005

    SYNVISC

    FDA Adverse Event
    Injury ·GENZYME CORPORATION·Product code MOZ·September 20, 2005

    AUTOPHERESIS C PLASMAPHERESIS INSTRUMENT, A200

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code GKT·September 2, 2005

    VUELOCK SCREW INSERTER

    FDA Adverse Event
    Malfunction ·EBI·Product code HXX·October 17, 2007

    6.2MM TI CLICK'X MONOAXIAL PEDICLE SCREW 50MM THRD LENGTH

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKB·April 21, 2010

    OPUSDUO

    FDA Adverse Event
    Injury ·LUMENIS·Product code GEX·April 13, 2006

    IAB : 8 FR - 40 CC

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DSP·August 31, 2005

    5.5MM TI CANCELLOUS LOCKING SCREW 26MM THRD LENGTH

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·September 29, 2005

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·September 2, 2005