BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    RUSCH BRILLANT SILICONE FOLEY CATHETER

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

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972184·posteriors; shade BL3; size M; upper jaw

    X-RAY SYSTEM FOR DENTAL APPLICATION

    FDA 510(k)
    FDA Class 2 ·Dental

    VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·May 8, 1997

    OXINIUM FEMORAL HEAD

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KWY·February 21, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 31, 2014

    DUROM US ACETABULAR COMPONENT 54/48 N

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·January 18, 2011