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

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    RAPIDVIT BLAST, RAPIDWARM BLAST

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

    Mini Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746108419·DB BKT MINI MS UR LAT 018 T+18 A+6 R=0

    Cutimed® Sorbion®

    FDA UDI
    BSN medical GmbH·04042809703238·CUTIMED SORBION BORDER STERILE 20X20CM 10

    Zavation

    FDA UDI
    Zavation LLC·00842166121591·K-Wire, Sharp, Threaded

    Zavation

    FDA UDI
    Zavation LLC·00842166121577·K-Wire, Blunt, Threaded

    Zavation

    FDA UDI
    Zavation LLC·00842166121584·K-Wire, Blunt, Smooth

    Zavation

    FDA UDI
    Zavation LLC·00842166121607·K-Wire, Sharp, Smooth

    JUP,P800 TO S800 & S102(PINS 2&5),Y CABLE,TEKTONE/AUSTCO WIRED

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828154819·JUP,P800 TO S800 & S102(PINS 2&5),Y CABLE,TEKTO...

    Zavation

    FDA UDI
    Zavation LLC·00842166181977·K-Wire, Blunt, Smooth

    Biliary Drainage Tube

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170046438·

    Zavation

    FDA UDI
    Zavation LLC·00842166185166·K-Wire, Blunt, Smooth

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694055284·Disposable Light Clip, Sterile

    SAFESTING AND SAFESTING HUB

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Z-NET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PROGAV®

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·January 3, 2018

    OT VERIO PRO METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

    ONE STEP BUTTON¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KGC·May 24, 2011

    THERMACHOICE

    FDA Adverse Event
    Malfunction ·GYNECARE WORLDWIDE·Product code MKN·July 30, 2008

    FULLY FLUTED REAMER 5.5MM

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HTO·February 16, 2023

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSE MANUFACTURING·Product code FKX·August 19, 2011