BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    SureMAX Family of Cervical Spacers

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Contrast Line

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333207435·Contrast Line 20"(50cm) M/F (Braided) 1200 PSI

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973530·

    RECLAIM MON REV LNG STEM 23 HO

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 3015516266·Product code LZO·September 22, 2025

    FINESSE ULTRA BREAST BIOPSY SYSTEM DRIVER (BLUE, PINK)

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

    1103 DIGITAL BLOOD PRESSURE MONITOR, MODEL LD 1103, 1133 DIGITAL BLOOD PRESSURE MONITOR, MODEL LD 1133

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEXTAR INFRARED CAMERA

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code JWH·September 10, 2021

    MIRU 1DAY UPSIDE (MIDAFILCON A)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·January 22, 2025

    RESOLUTION CLIP DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MND·October 7, 2008

    ARMADA 14 PTA CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LIT·June 27, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 5, 2011