BEUDAMED
    168 results · 25ms · Sources: EU EUDAMED, US FDA

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    BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964152238·Endo Carry-on Procedure Kit contains Basin, Enz...

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890108090·Zirlux Multi Impr Coping

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR50108091·Weingart universal lightwire plier

    Humelock II Cemented Reversible Shoulder

    FDA UDI
    FX SOLUTIONS·03701037308479·TRIAL HUMERAL CUP STANDARD Ø32+9

    Single Use Biliary Stent V

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170185878·Single Use Biliary Stent V

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100090·Dilator Sleeve, Screwdriver

    REAL PATIENT WIRELESS AMBULATORY EEG, MODEL EX-AMB-WIRELESS-RP (PROPOSED)

    FDA 510(k)
    FDA Class 2 ·Neurology

    KOKO PEAK KP; KOKO PEAK KP+

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·May 1, 2018

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

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    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 19, 2013

    VASOVIEW 7XB EVH SYSTEM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 2, 2011

    RIATA ST ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026