BEUDAMED
    25 results · 29ms · Sources: EU EUDAMED, US FDA

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    FOLEY CATHETER

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

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551202524·COLLIN Tongue Seizing Forceps

    Bardia® Coude Olive Tip Urethral Foley Catheter

    FDA UDI
    C. R. Bard, Inc.·00801741039058·Bardia® Coude Olive Tip Urethral Catheter

    TEKNO®

    FDA UDI
    Tekno-Medical Optik-Chirurgie GmbH·04044684004684·STANDARD SCISSORS STRAIGHT FIG. 3 16,5CM

    TEKNO®

    FDA UDI
    Tekno-Medical Optik-Chirurgie GmbH·04044684207344·STANDARD SCISSORS STRAIGHT FIG. 3 16,5CM

    ACUMED

    FDA UDI
    Acumed LLC·10806378097898·2.0mm / 2.7mm Drill Guide

    Rampart-O

    FDA UDI
    SPINEOLOGY INC.·M7402802516·Rampart-O

    Rampart-O

    FDA UDI
    SPINEOLOGY INC.·M9403802516·Asm, Rampart-O

    Rampart-O

    FDA UDI
    SPINEOLOGY INC.·M7403802516·Asm, Rampart-O

    PERI-LOC PERIARTICULAR LOCKED PLATING SYSTEM HEXALOBULAR BONE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LUCINA MODEL MELODI

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

    BARDIA® COUDE OLIVE TIP URETHRAL CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·November 13, 2025

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·June 2, 2022

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·June 28, 2024

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·June 28, 2024

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·December 13, 2024

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·October 8, 2024

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·May 9, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 19, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·May 26, 2015