BEUDAMED
    30 results · 30ms · Sources: EU EUDAMED, US FDA

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    NAT - NUCLEIC ACID TRANSPORT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092127285·Multi-Unit Non-Engaging Titanium Base w/ SRA Screw

    Preat Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092165393·Multi-Unit Titanium Base w/SRA Screw Kit contai...

    STATLYTE NA/K/CL/LI ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    FRESNIUS HEMOFLOW F7NR, F50NR, F70NR HEMODIALYZERS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PENUMBRA SMART COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·August 12, 2022

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DXY·August 11, 2011

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 19, 2024

    COATED VICRYL RAPIDE (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·March 14, 2013

    UNKNOWN ZIMMER CR FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 24, 2011

    NEXGEN COMPLETE KNEE SOLUTION FLEXION BALANCING INTRUMENTATION FEMORAL ANTERIOR/

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code KWY·February 22, 2008

    ENRHYTHM

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NVZ·December 12, 2011

    BIOMET TAPERLOC FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 5, 2018

    TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 4, 2016

    TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 4, 2016

    TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 4, 2016

    BIOMET COCR FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 5, 2018

    OPTIFLUX 180NR DIALYZER FINISHED ASSMBLY

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·July 21, 2018

    IMPLANT MOUNT 3.4MM(D) X 15MM(L)

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NDP·April 26, 2019

    OPTIFLUX 180NRE DIALYZER FINISHED ASSMBLY

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·August 13, 2018