BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    IM-9A MICROINJECTORS

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

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040044452·Elevator Potts Cross Bar #1

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496001911·MAGIC 70, SIZE S, BLU SCURO, GRADUATED COMPRESS...

    Mariner MIS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981255817·Diamond Stylet, Navigation

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180172258·MALIS FORCEPS, TITATNIUM, BAYONET, 8.5"

    CastleLoc Pectus Bar System Instrument Set

    FDA UDI
    L&K BIOMED CO. ,LTD.·08809986488688·Screw Thread Connector

    BD SYRINGE LUER-LOK TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·March 14, 2019

    PANORET, MODEL 1000A

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MICROGRASP BIPOLAR COAGULATOR, MODELS 90048-90057

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    HS III PROXIMAL SEAL SYTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·February 12, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIQ·February 27, 2011

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 21, 2008

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    4.5 HEALIX ADVANCE BR W/OCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·December 30, 2025

    INTACS CORNEAL IMPLANTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    HEALIX ADVANCE ORTHOCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 27, 2026

    HEALIX ADVANCE ORTHOCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 9, 2026

    4.5 HEALIX ADVANCE BR W/OCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·January 29, 2026