BEUDAMED
    10 results · 19ms · 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 ×

    TEXTURED POWDER-FREE LATEX EXAMINATION GLOVES WITH ALOE VERA GREEN, CONTAINS 50 MCGM OR LESS OF TOTAL WATER EXTRACTABLE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111024·INSTRUMENT CADDY MEDIUM

    Stainless Steel

    FDA UDI
    Seaspine Orthopedics Corporation·10889981114848·Poly Screw Sterilization Case

    POWDER FREE NITRILE EXAMINATION GLOVES, ORANGE (ORANGE SCENTED), WHITE (VANILLA SCENTED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DynaCAD

    FDA 510(k)
    FDA Class 2 ·Radiology

    ASAHI APS DIALYZERS

    FDA Adverse Event
    Injury ·ASAHI KASEI MEDICAL CO., LTD.·Product code KDI·March 1, 2013

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·February 15, 2011

    VIRTUOSO

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

    MD HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·August 26, 2022

    PT HYBRID GLEN POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·December 8, 2022