BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327371109·FACIAL ID-TRAUMA-1PLATE, KIT

    INSTRUSAFE

    FDA UDI
    Summit Medical, Inc.·00385640008785·

    INSTRUSAFE

    FDA UDI
    Summit Medical, Inc.·00385640008792·

    MAGO 4S

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Omnifix Low Dead Space Luer Lock Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OMNIFIX®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FMF·March 6, 2026

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 25, 2014

    POLIGRIP

    FDA Adverse Event
    Injury ·GLAXOSMITHKLINE·Product code KOL·November 2, 2010

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 27, 2012

    Boston Scientific PT2 Light Support Guide Wire 185cm J-Tip, Catalog Number 38931-01. Sold in single pack and 5-pack. PTCA Guide Wire with Hydrophilic Coating. Boston Scientific Guide Wires are steerable guide wires available in a variety of lengths and diameters. The distal tip is shapeable, or, alternatively, is available in a preshaped ''J'' tip. Made in USA.

    FDA Recall
    Terminated ·Boston Scientific·Product code DQX·August 31, 2006