BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Infrared Forehead Thermometer (Model IR-FT)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENDOSCOPIC CYTOLOGY BRUSHES

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

    NCB, FEMUR PLATE, RIGHT, 9 HOLES, 246 MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·March 28, 2019

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·February 4, 2014

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 5, 2010

    LINOX S 65

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·November 21, 2012

    Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD, Inc.·March 19, 2025