BEUDAMED
    42 results · 29ms · Sources: EU EUDAMED, US FDA

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    DESTINO TWIST, STEERABLE GUIDING SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768505·GENUMEDI PSS GREEN VI

    AGILITY

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295035442·AGILITY LP TOTAL ANKLE SYSTEM TALAR SIZE 6 RIGH...

    AGILITY

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295035473·AGILITY LP TOTAL ANKLE SYSTEM TALAR SIZE 6 LEFT...

    FORA V20 BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    POLYMER COATED, CHLORINATED, POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING (LESS THAN 50 UG/G PER GLOVE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981441395·ALIF Paddle Distractor 6mm, 7°

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    INGEVITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 3, 2014

    AUTOPLEX SYSTEM W/ VERTAPLEX W/O NEEDLES

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-PUERTO RICO·Product code JDZ·May 31, 2013

    REMB SAG SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·June 17, 2011

    KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012