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

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    DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Ponto

    FDA UDI
    Oticon Medical AB·05712149013937·Ponto Soft band, pink

    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

    EI DOWNPAK BARRIER SLEEVES

    FDA 510(k)
    FDA Class 1 ·Dental

    VAULT ALIF 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

    LUMINOS LOTUS MAX

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·March 5, 2025

    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

    DUR MAR 10D LNR 32IDX60OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC./REG. #1818910·Product code LPH·June 17, 2013

    SWEET TIP

    FDA Adverse Event
    Injury ·HISTORICAL PUERTO RICO·Product code NVN·July 23, 2011

    PROSIMA PELVIC FLOOR REPAIR KIT

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·September 22, 2008

    NEXGEN PROVISIONAL ARTICULAR SURFACE

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HWT·February 26, 2020

    VANGUARD MONO FINNED STM TIB 71X14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JWH·December 9, 2024

    VANGUARD ROCC TIB BRG UHMWPE 60X10MM

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JWH·September 16, 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

    MUST MINI POLYAXIAL SCREW 3.5 X 20 FULL THREAD + NUT

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