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

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    BiZact Tonsillectomy Device Advanced Bipolar Tissue Sealer/Divider

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

    Contrast Line

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333207404·Contrast Line 30"(75cm) Female/Rotating Adapter...

    PRUITT CAROTID KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOLOGIC VISCERAL FAT SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD LUER-LOK DISPOSABLE SYRINGE WITH BD LUER-LOK TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·May 22, 2019

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 20, 2025

    PROLIEVE THERMODILITATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 7, 2008

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 27, 2013

    UNK - SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·July 29, 2011

    SYRINGE 3ML LL 200 S/C

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·June 14, 2019

    PEDICLE SCREW 03.50.054 PEDICLE SCREW 8X40MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·June 16, 2023

    Boston Scientific Fetch 2 Aspiration Catheter, Catalog No. 109400-001. Product The Fetch 2 Aspiration Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the peripheral and coronary vasculature.

    FDA Enforcement
    Class I ·Terminated·Boston Scientific Corporation·April 27, 2016