BEUDAMED
    11 results · 31ms · 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.

    EZ MANAGER MAX DIABETES MANAGEMENT SOFTWARE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014606392·MIDMARK CHIC CST 2" DELUXE

    NA

    FDA UDI
    STRYKER CORPORATION·07613327058574·Insert, Oviduct Forceps

    AMISTEM H CEMENTLESS STEM SIZE 2 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 29, 2015

    SHUTTLE STOP

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

    ACTIVEECG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC.·Product code NDN·February 26, 2010

    VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I ES REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·April 26, 2013

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·April 22, 2011

    RADIX ANKER

    FDA Adverse Event
    Malfunction ·DENTSPLY MAILLEFER·Product code ELR·July 17, 2008

    Mercury Spinal System DIA 5.5 x 80 MM Lordosed Rod, Part Number: 60100-080. Intended to provide immobilization and stabilization of the spine in skeletally mature patients.

    FDA Enforcement
    Class III ·Terminated·Spinal Elements, Inc·May 15, 2013