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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    BIO-PROBE TRANSDUCER (ADULT)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO INTRACYTOPLASMIC SPERM INJECTION (ISCI), MICRO-INJECTION PIPETTES, HOLDING PIPETTES, DENUDING PIPETTES,

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BACTEC Lytic/10 Anaerobic/F Culture Vials (plastic)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·May 29, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 12, 2011

    SURGITEK HIGH PROFILE LO BLEED

    FDA Adverse Event
    Injury ·MEDICAL ENGINEERING CORP.·Product code FTR·August 22, 2008

    BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 18, 2021