BEUDAMED
    36 results · 23ms · Sources: EU EUDAMED, US FDA

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    FLEXITIME XTREME 2 HEAVY TRAY CARTRIDGE REFILL, FEXITIME XTREME 2 LIGHT TRAY CARTRIDGE REFILL

    FDA 510(k)
    FDA Class 2 ·Dental

    X-OMAT MX Developer and Replenisher

    FDA UDI
    CARESTREAM HEALTH, INC.·60889971101617·X-OMAT MX Developer and Repl 38L

    Sklar

    FDA UDI
    SKLAR CORPORATION·50649111357846·SKLAR DISINFECTANT WIPES CS/12

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383554329·Gutta Percha Points is used to root canal filin...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383501903·Gutta Percha Points is used to root canal filin...

    LIFEJET PRINTER 400

    FDA 510(k)
    FDA Class 2 ·Radiology

    MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DELTAFILL18 8MM X 35CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·July 29, 2020

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 30, 2013

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·September 12, 2013

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code BRZ·September 13, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 17, 2013

    NDEHP Y-BLOOD SET W/FILTER PUMP 203CM

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 24, 2011

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 10, 2013

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code LZH·April 30, 2013

    UNK SERI SURGICAL SCAFFOLD

    FDA Adverse Event
    Injury ·ALLERGAN·Product code OXF·August 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 11, 2011

    SOLUSET 100X60

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 22, 2013