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

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    Filters Regulation: Us FDA ×

    Altus Spine Titanium Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10887488578668·STERILE CAUDAL TRAY

    SR PIP

    FDA UDI
    Stryker GmbH·00886385019888·SIZE 5: PIP PROXIMAL BROACH ASSEMBLY (RED)

    M.U.S.T. MINI POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·August 27, 2025

    MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·April 6, 2018

    MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·March 8, 2022

    SYNERGY CT PICC

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NUVASIVE HELIX ACP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MUST MINI ROD TI 3.5 X 80MM (STERILE)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 13, 2021

    MUST MINI MUST MINI POLYAXIAL SCREW 3.5 X 24 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 14, 2020

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 14, 2013

    PCA MTK TIB/INS SMALL 7 LEFT OBSOLETE PRODUCT NO

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·July 15, 2011

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008

    HANDPIECE BOX OF 10

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HAM·February 13, 2019

    VERSAFITCUP DM DOUBLE MOBILITY HC LINER Ø 52/28

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·August 9, 2023

    MUST MINI POLYAXIAL SCREW 3.5 X 18 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·October 27, 2022

    EVEREST ® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·STRYKER-SPINE·Product code LXH·September 9, 2019

    MUST MINI ROD REDUCTION DEVICE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·September 27, 2019

    M.U.S.T. MINI POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·August 11, 2025

    MUST MINI POLYAXIAL SCREW 3.5 X 20 FULL THREAD + NUT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWP·February 2, 2018