BEUDAMED
    9 results · 18ms · 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 ×

    UTERINE INJECTOR WITH SPRING

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

    LIQUICHEK HEMATOLOGY CONTROL (A)

    FDA 510(k)
    FDA Class 2 ·Hematology

    DENTIUM IMPLANTIUM AND SUPERLINE ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    ASCERTA¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code FGE·February 4, 2013

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 29, 2010

    HI-TORQUE WHISPER MS GUIDE WIRE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code DQX·July 17, 2014

    BD SYRINGE ALLERGY 1ML W/NDL 27X1/2 RB

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·July 10, 2019

    BD SYRINGE ALLERGY 1ML W/NDL 27X1/2 RB

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·July 10, 2019

    BD PRECISIONGLIDE SYRINGE ALLERGY 1ML W/ NEEDLE 28X1/2 RB

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·May 31, 2019