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

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    CARDIAC OUTPUT KIT, MODEL CO-1 & INLINE SENSOR CABLE, MODEL ILS-1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694000314·2.0mm x 4mm Screw

    DELTA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540337467·DELTA 2.2X4MM SCREW, 1 EA

    18M - Five Star Safety

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588220048·18M - Five Star Safety

    18M - Five Star Safety - w/Logo

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620046·18M - Five Star Safety - w/Logo

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694028714·2.0mm x 4mm Screw, Sterile

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694054287·2.0 x 4mm Screw Sterile Qty 10

    MONTANE ALPS M-P5.F0 [SZER 69 CM] US

    FDA UDI
    MEDEN INMED SP Z O O·05903684802043·The MONTANE treatment table is a treatment tabl...

    EASY GUIDE ELECTROSURGICAL ACCESS DEVICE

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

    ZYBIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLARION

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS CORP.·Product code MCM·March 12, 2004

    CLARION

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS CORP.·Product code MCM·March 11, 2004

    MAYFIELD RADIOLUCENT SYSTEM

    FDA Adverse Event
    Other ·SCHAERER MAYFIELD USA, INC.·Product code HBL·March 22, 2004

    TACHOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code MRM·February 11, 2004

    29 GA PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMI·March 10, 2004

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 21, 2020

    5.5 MM TI CANCELLOUS LOCKING SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·May 6, 2004

    POLYSORB 2/0

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GAM·October 25, 2004

    ULTRACISION SURGICAL DEVICE, CURVED SHEARS, ENDO

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.·Product code GEI·November 1, 2004

    POLYSORB 0

    FDA Adverse Event
    Injury ·US SURGICAL·Product code GAN·October 25, 2004