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

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    Disposable Electrosurgical Pencils

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

    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

    POWDER-FREE NITRILE GLOVES, BLACK

    FDA 510(k)
    FDA Class 1 ·General Hospital

    REGENERX RINGLOC + MODULAR ACETABULAR SHELLS

    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

    RINGLOC RIMCUP SHELL

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code LPH·August 31, 2017

    PFC KEEL TIB TRAY CEM SZ2

    FDA Adverse Event
    Injury ·DEPUY IRELAND ¿ REG. # 9616671·Product code JWH·April 7, 2014

    PFC SIGMA CRVD INSERT SZ2 10MM

    FDA Adverse Event
    Injury ·DEPUY IRELAND ¿ REG. # 9616671·Product code JWH·April 7, 2014

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 20, 2011

    EEA 31MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC·Product code GDW·June 7, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 10, 2008

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    MIH MOD CUP INSERTER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LXH·August 17, 2017

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025

    MUST MINI POLYAXIAL SCREW 3.5 X 18 FULL THREAD + NUT

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

    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