BEUDAMED
    9 results · 26ms · 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.

    BRUCELLA MEDIA

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DD cube ONE ML

    FDA UDI
    Dental Direkt GmbH·EDDIG8340061·DD cube ONE® ML are dental mill blanks made fro...

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024154025·

    AllSource Drug Detector FenTest; AllSource Drug Detector Fentanyl Test

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DISPOSABLE LAPAROSCOPIC ELECTRODE, DISPOSABLE LAPAROSCOPIC ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL GUIDE WIRE

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·May 27, 2014

    TI 12-POINT NUT-11MM

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·November 15, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·September 14, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018