BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    SYPHER SPACER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Biomet® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304233096·

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037961·Unitek(TM) Bicuspid Band General Purpose Wide U...

    SPI VARIOMULTI ANGLED ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    ATALIA TITANIUM SURGICAL MESH

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 29, 2026

    UNSPECIFIED PRIMARY PLUM SET

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·October 3, 2024

    BELT CLIP PUMP CLEAR

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    BLAKE DRAIN

    FDA Adverse Event
    Injury ·ETHICON, INC·Product code KOG·June 27, 2011

    UNSPECIFIED PRIMARY PLUM SET CLAVE PORT, CLAVE Y-SITE, SECURE LOCK

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·November 24, 2024

    TECNIS SIMPLICITY

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·February 7, 2023