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

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    UMI X-RAY FILM CASSETTE

    FDA 510(k)
    FDA Class 2 ·Radiology

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623867·PEEK Corp Core, Ø14x31mm

    GLOBUS GENESY 1100 STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HAART 200 Aortic Annuloplasty Device 19mm, HAART 200 Aortic Annuloplasty Device 21mm, HAART 200 Aortic Annuloplasty Device 23mm, HAART 200 Aortic Annuloplasty Device 25mm

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·April 30, 2026

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·December 3, 2025

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·October 16, 2025

    PISCES QUAD PLUS

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., VILLALBA·Product code GZB·February 27, 2007

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 31, 2014

    INTRAMATIC CONTRA ANGLE 23 A

    FDA Adverse Event
    Injury ·KAVO DENTAL GMBH·Product code EFB·January 17, 2011

    HAART 200 AORTIC ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·May 8, 2025

    HAART 200 AORTIC ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·CORCYM INC.·Product code KRH·May 9, 2025