BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    SEMI COMPLIANT (SC) 35 BALLOON DILATATION CATHETER

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

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993303·anteriors; shade C1; mould BS

    Cutimed® Sorbact®

    FDA UDI
    BSN medical GmbH·04042809464351·CUTIMED SORBACT HYDROACTIVE BORDER STERILE 19X1...

    SCOUTPRO 7F LONG CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Tinnitus Sound Generator Module

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CONSULT HCG TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·March 4, 2025

    SYNERGY¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 4, 2015

    LOGIC CR TIB INSERT STD, SZ 2.5, 9 MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·May 3, 2023

    ABSOLUTE PRO .035 SELF EXPANDING STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code FGE·March 7, 2013

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 7, 2011