BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    TX-4(TENS) (SIGMA TENS)

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809916493225·Multi-Axial Fenestrated Screw, Ø4.5 x 50mm, Ø6....

    EMIT ST SERUM TRICYCLIC ANTIDEPRESSANT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HOBBS MEDICAL/JAYCO ASPIRATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    7600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 22, 2014

    CAPSURE SP NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010

    VERITAS COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·December 15, 2012

    PEG FULLY THREAD 2.5MM X 22

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRS·December 16, 2025

    PEG FULLY THREAD 2.5MM X 18

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRS·December 16, 2025

    PEG SCREW 2.5MM X 18MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRS·December 16, 2025

    PEG SCREW 2.5MM X 20MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRS·December 16, 2025

    CORONOID PLATE RT ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRS·December 16, 2025