BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    NON-INVASIVE TUBING

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517394538·CoRoent® XL Wide, 14x22x50mm Lordotic

    i-ED COIL

    FDA UDI
    KANEKA CORPORATION·04540778177239·The i-ED COIL is used for vascular embolization...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150577·K-WIRE - DOUBLE TROCAR 1.4mm DIA x 125mm

    CLINPRO PROPHY POWDER

    FDA 510(k)
    FDA Class 2 ·Dental

    Phosphoric Acid Etching Gel

    FDA 510(k)
    FDA Class 2 ·Dental

    TRILOGY SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER·Product code LPH·January 9, 2013

    CAPSURE SENSE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DTB·December 13, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 6, 2014

    BIOMET StageOne Knee Femoral Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 432175.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020