BEUDAMED
    14 results · 23ms · Sources: EU EUDAMED, US FDA

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    VITRUVIAN ULTIMATE ASPIRATOR

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528104132·Drill Sleeve, 6.5/7.0 Cannulated Screws

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071134686·16FR x 1.7 cm x 22 cm Low Profile Transgastric-...

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071102166·16FR x 1.7 cm x 22 cm Low Profile Transgastric-...

    BLOXX RAPID CLOTTING AGENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    ALYTE Y-MESH GRAFT

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

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071117092·16FR x 1.7 cm x 22 cm Low Profile Transgastric-...

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071134693·16FR x 1.7 cm x 22 cm Low Profile Transgastric-...

    PROTECTA XT CRT-D

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014

    ATRICLIP GILLINOV-COSGROVE LAA EXCLUSION SYS.

    FDA Adverse Event
    Death ·ATRICURE, INC.·Product code FZP·June 6, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 27, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·January 8, 2009

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·November 26, 2025

    Fortify Assura, Sterile EO, Model #/ Part #: CD1257-40/100042322, 100059623; CD1257-40Q/100042341, 100059535; CD1259-40/100041914, 100042338, 100059536, 100059646, 100081567; CD1259-40Q/100041931, 100042339, 100059537, 100059620, 100059626, 100078685; CD1263-40/100042948; CD1263-40Q/100042949; CD1357-40C/100080365, 100080377, 100083441; CD1357-40Q/100080389, 100080390, 100083388; CD1359-40/100078740, 100083267, 100096839; CD1359-40C/100078500, 100078969, 100079372, 100079373, 100083442, 100083443, 100117545; CD1359-40Q/100078804, 100079155, 100079413, 100083445, 100096884; CD1359-40QC/100078603, 100079145, 100079146, 100079239, 100083405, 100083444, 100117632, 100127000, 100127065; CD1363-40C/100080349; CD1363-40Q/100080317; CD1391-40C/100080756; CD1391-40QC/100080783; CD2257-40/100042337, 100059839; CD2257-40Q/100042342, 100059842; CD2259-40/100041893, 100042308, 100059794, 100059907, 100082567; CD2259-40Q/100041894, 100042309, 100059845, 100059873, 100078610; CD2263-40/100042950; CD2263-40Q/100043201; CD2357-40C/100080404, 100080413, 100083490; CD2357-40Q/100080319, 100080412, 100083492; CD2359-40/100078750, 100083466; CD2359-40C/100078651, 100079201, 100079240, 100079442, 100083501, 100083502, 100117546; CD2359-40Q/100078841, 100079109, 100083472; CD2359-40QC/100078652, 100079156, 100079157, 100079337, 100083407, 100083465, 100117580, 100127092, 100127103; CD2363-40C/100080416; CD2363-40Q/100080407; CD2391-40C/100080784; CD2391-40QC/100080744

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018