BEUDAMED
    87 results · 22ms · Sources: EU EUDAMED, US FDA

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    SMV Scientific Bone Plate and Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    22MM COMPACT BREATHING SYSTEM WITH 3L BAG, LUER ELBOW AND LIMB, 2M

    FDA UDI
    Intersurgical Incorporated·05030267063352·22MM COMPACT BREATHING SYSTEM WITH 3L BAG, LUER...

    Line

    FDA UDI
    MECTRA LABS, INC.·00817984011041·Dual Spike Saline

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702450385·Elvarex 2/Thigh High/Slant-Open Toe/Dotted Sili...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04059993426560·ELVAREX 1/KNEE HIGH/SLANT-CLOSED TOE/SOFTFIT-SL...

    Phantom Hindfoot TTC/TC Nail System

    FDA UDI
    Paragon 28, Inc.·00889795135964·Phantom 2.0 ActivCore Nail, 11.5 X 200mm

    Phantom Hindfoot TTC/TC Nail System

    FDA UDI
    Paragon 28, Inc.·00889795097750·Phantom ActivCore Nail, 11.5 X 200mm

    Phantom Hindfoot TTC/TC Nail System

    FDA UDI
    Paragon 28, Inc.·00889795135872·Phantom ActivCore Nail, 11.5 X 200mm

    Phantom Hindfoot TTC/TC Nail System

    FDA UDI
    Paragon 28, Inc.·00889795118080·Phantom ActivCore Nail, 11.5 X 200mm Sterile Pa...

    IMAGYS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARCHITECT CA 19-9XR ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 4, 2019

    ARCHITECT CA19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·October 31, 2025

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 19, 2026

    CD004, 12/15MM RETRIEVAL SYSTEM, 5/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL·Product code GCJ·October 8, 2014

    MAXIMO VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 7, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 1, 2026

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026