BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    ONE-WAY VALVE-FEMALE, M-503

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UROFLOW-CYSTOMETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RIA, QUANTIMUNE E3

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 6, 2014

    MODEL NOT SPECIFIED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·October 15, 2012

    OCTRODE 3/4 PERCUTANEOUS LEADS

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·August 4, 2010

    G7 OSSEOTI 4 HOLE SHELL 56MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 27, 2020

    G7 DUAL MOBILITY LINER 44MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 27, 2020

    SPIDER FX

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NTE·July 30, 2020

    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 280 mm, Item Number: 814609280

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 19, 2018

    FEMORAL STEM 12/14 NECK TAPER PLASMA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 27, 2020

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025