BEUDAMED
    21 results · 20ms · Sources: EU EUDAMED, US FDA

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    Agile Esophageal Stent System

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

    LeMaitre Embolectomy Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663101030·4F 40 cm NovaSil Silicone Single Lumen Embolect...

    Super Upper Limbs Versalock Plating System

    FDA UDI
    GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258665672·VERSALOCK WRIST FUSION PLATE - LONG ANGULATED D...

    LeMaitre Embolectomy Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663100910·4F 40 cm NovaSil Silicone Single Lumen Embolect...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013785·Multi thread Cannulated Ø5x45

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013747·Multi thread Cannulated Ø5x35

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013808·Multi thread Cannulated Ø5x50

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013792·Multi thread Cannulated Ø5x45 RBM

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034384·Multi thread Cannulated Ø5x30 RBM

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013761·Multi thread Cannulated Ø5x40

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013778·Multi thread Cannulated Ø5x40 RBM

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013754·Multi thread Cannulated Ø5x35 RBM

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361013815·Multi thread Cannulated Ø5x50 RBM

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034377·Multi thread Cannulated Ø5x30

    THERMO SCIENTIFIC QMS EVEROLIMUS REAGENTS, CALIBRATORS AND CONTROLS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MANDREL GUIDEWIRES OR M-WIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIFEPAK® 35 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·January 29, 2026

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·July 27, 2011

    POSEY KEEPSAFE DELUXE

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·June 4, 2013

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·September 26, 2008