BEUDAMED
    15 results · 26ms · Sources: EU EUDAMED, US FDA

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    PALABOND

    FDA 510(k)
    FDA Class 2 ·Dental

    Class B 21 Plus - 36 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588244228·Class B 21 Plus - 36 Metal

    Votion®

    FDA UDI
    Ortho Organizers, Inc.·00190707115036·Votion .022 R LL4 G/O -17T 0A 4DO (10PK)

    Pinnacle®

    FDA UDI
    Ortho Organizers, Inc.·00190707113100·Pinnacle .022 R LL4 G/O -17T 0A 4DO (10PK)

    Votion

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730009333·Votion .022 R LL4 G/O -17T 0A 4DO (10PK)

    Pinnacle

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730011169·Pinnacle .022 R LL4 G/O -17T 0A 4DO (10PK)

    DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    B-D INTERLINK SYRINGE CANNULA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRUETRACK

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code CGA·July 16, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    NEXGEN LEGACY LPS-FLEX ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·December 7, 2010

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011