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

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    Breast BI 7 MR Coil 1.5T Mammavention

    FDA 510(k)
    FDA Class 2 ·Radiology

    Super Upper Limbs Versalock Plating System

    FDA UDI
    GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258663616·VERSALOCK “Y” DISTAL ULNA MINI PLATE 115.0mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011590·PedFuse Respond, CNL, 7.0mm x 50mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011552·PedFuse Respond, CNL, 7.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011613·PedFuse Respond, CNL, 7.0mm x 60mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011637·PedFuse Respond, CNL, 7.0mm x 70mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011576·PedFuse Respond, CNL, 7.0mm x 40mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011583·PedFuse Respond, CNL, 7.0mm x 45mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011620·PedFuse Respond, CNL, 7.0mm x 65mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011606·PedFuse Respond, CNL, 7.0mm x 55mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011651·PedFuse Respond, CNL, 7.0mm x 80mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011644·PedFuse Respond, CNL, 7.0mm x 75mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361011569·PedFuse Respond, CNL, 7.0mm x 35mm

    TWIST DRILL

    FDA UDI
    Biomet Orthopedics, LLC·00887868017643·

    NA

    FDA UDI
    STERILMED, INC.·10888551009478·DRILL BIT STAINLESS STEEL

    APOLOWAKO HBA1C, GLUCOSE AND ANALYZER, MODELS 993-24601, 991-24401 AND 993-25201

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACUMED WRIST ARTHRODESIS PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OLYMPUS EMPOWER H65

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022

    STYLE 68 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·March 31, 2025

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019