BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    Access25™ Delivery Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MITEK

    FDA UDI
    Medos International Sàrl·10886705029068·Sheath with 1 Rotating Stopcock compatible with...

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295122616·REV INST STERILIZATION TRAY UPPER

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL COMPANY·Product code OAD·June 25, 2010

    HOVEROUND POWER WHEELCHAIR, MODEL HD700

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VERIGENE ENTERIC PATHOGEN NUCLEIC ACID TEST (EP)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 9, 2011

    PROXIMATE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·November 17, 2008

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·May 28, 2025