BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    WAKO CPK TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DD cube ONE ML

    FDA UDI
    Dental Direkt GmbH·EDDIG8320041·DD cube ONE® ML are dental mill blanks made fro...

    REZNICK MEMBRANE HOLDING FORCEPS

    FDA UDI
    W.H. Holden, Inc.·D9288320040·

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153530·

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 10, 2009

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 10, 2009

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 10, 2009

    AQUABOSS ECORO DIA 50

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NPWT WOUND DRESSING KIT- MEDIUM, NPWT WOUND DRESSING KIT- LARGE

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

    KARL STORZ

    FDA Adverse Event
    Injury ·KARL STORZ ENDOSCOPY·Product code KQT·January 21, 2004

    INTELEPACS

    FDA Adverse Event
    Malfunction ·INTELERAD MEDICAL SYSTEMS INCORPORATED·Product code LLZ·March 7, 2014

    N/A

    FDA Adverse Event
    Malfunction ·STRYKER SUSTAINABILITY SOLUTIONS·Product code NLQ·November 14, 2012

    V-LOC 180 ABS CLOS DEVICE 3-0 CL 18 P-12

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GAM·September 8, 2010