BEUDAMED
    130 results · 26ms · Sources: EU EUDAMED, US FDA

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    FETAL DOPPLER JPD-100S

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

    TRESTLE LUXE

    FDA UDI
    ALPHATEC SPINE, INC.·00190376215143·TRESTLE LUXE II, ACP, 1-LEVEL, 24

    Aspida

    FDA UDI
    ALPHATEC SPINE, INC.·00190376115955·24mm LUMBAR PLATE, TF

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989028188·SS BROAD ARCH ROUND140 LO LGE PK/20

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450160053·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450160107·

    Visensia

    FDA UDI
    OBS MEDICAL LIMITED·05060457930010·Visensia® software is a computerized analysis s...

    FASTX STERNAL INTRAOSSEOUS DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARTHREX UNIVERS 30 SHOULDER PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·September 15, 2011

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 25, 2025

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·April 22, 2025

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·April 28, 2025

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·August 18, 2025

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·November 22, 2024

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·February 15, 2005

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·August 26, 2025

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015