BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    OSFERION D

    FDA 510(k)
    FDA Class 2 ·Dental

    DERMAGRIP AND MULTIPLE POWDER FREE LATEX EXAMINATION GLOVES, STERILE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAM O

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SEREINE EXTRA STRENGTH DAILY CLEANER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·July 1, 2010

    ESPRIT¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code NXW·August 6, 2025

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·September 30, 2013

    12MM/130 DEG TI CANN TROCH FIXATION NAIL 235MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HSB·April 29, 2013

    DISPOSABLE SUTURE PLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code FHQ·May 9, 2011

    SILHOUETTE 20 HF

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code IZO·July 25, 2008