BEUDAMED
    29 results · 24ms · Sources: EU EUDAMED, US FDA

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    CLEAR VISION EMBRYO TRANSFER CATHETER SET, MODEL B100000 - B 100007; CLEAR VISION TRIAL TRANSFER CATHETER SET

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Premier K-FILES

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·D6919053208·FILES PKG 6 21MM 40

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809841831·FOR MEN 30-40 MM HG KNEE HIGH CLOSED TOE LARGE-...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065814·EXTRAORAL ELASTICS 3/16" 8 oz

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0132080·Trial, TLIF, 27L OB CRV 7Deg, 8mm

    R & D 3K RETIC

    FDA 510(k)
    FDA Class 2 ·Hematology

    CEDIA CYCLOSPORINE PLUS ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    BACT/ALERT® BPA US CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MZC·June 24, 2019

    SYNCHRO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·April 11, 2013

    STERRAD NX STERILIZATION SYSTEM

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·May 28, 2008

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·April 13, 2011