BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    GALACTOSID-ASE TUBES

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AO USB RECEIVER, WI-BOX, WI-BOX PSU KIT, WI-BOX XPRESS CABLE, PW USB RECEIVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TOKUYAMA M-BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 30, 2007

    REVEAL XT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·October 31, 2012

    6.5CM ADULT CRANI ATTACHMT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 11, 2013

    Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05, 13894-16, 17550-08, 12236-18, 11854-15, 8043-29, 12466-17, 15599-17, 14764-09, 13194-16, 17069-09

    FDA Recall
    Open, Classified ·Alcon Research LLC·Product code LRO·February 10, 2025

    Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05, 13894-16, 17550-08, 12236-18, 11854-15, 8043-29, 12466-17, 15599-17, 14764-09, 13194-16, 17069-09

    FDA Enforcement
    Class II ·Ongoing·Alcon Research LLC·March 12, 2025