BEUDAMED
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    Microstream Advance

    FDA UDI
    ORIDION MEDICAL 1987 LTD.·20884521761565·Adult Oral-Nasal CO2 Filter Line with O2 connec...

    ITREL 3

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code LGW·March 7, 2013

    MVA PUMP TUBING

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·November 17, 2011

    IPAS MVA PLUS

    FDA Adverse Event
    Death ·WOMANCARE GLOBAL·Product code HHI·July 7, 2010

    TRINICA CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWQ·March 20, 2008

    IPAS MVA PLUS ASPIRATOR

    FDA Adverse Event
    Death ·WOMANCARE GLOBAL·Product code HHI·May 26, 2010

    IPAS MVA PLUS ASPIRATOR

    FDA Adverse Event
    Injury ·WOMANCARE GLOBAL·Product code HHI·March 23, 2026

    FEMORAL HEAD

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 10, 2021

    MAY PLATE/9 HOLE

    FDA Adverse Event
    Injury ·LINK AMERICA·Product code HRS·August 1, 1994

    35-X PROFLEXX

    FDA Adverse Event
    Malfunction ·FERNO-WASHINGTON, INC.·Product code FPO·February 10, 2021

    WomanCare Global Ipas MVA Plus Aspirator

    FDA UDI
    WOMANCARE GLOBAL TRADING, INC.·00853615006260·The device is used to evacuate the contents of ...

    PERMOBIL C300

    FDA Adverse Event
    Malfunction ·PERMOBIL INC.·Product code ITI·March 26, 2018

    SIMS DELTEC CADD PRIZM

    FDA Adverse Event
    Death ·SMITHS MEDICAL ASD, INC.·Product code FRN·May 25, 2023

    SPHERX DEFORMITY SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code NKB·July 25, 2014

    TOTAL TMJ IMPLANTS

    FDA Adverse Event
    Other ·TMJ IMPLANTS, INC.·Product code LZD·April 26, 2010

    NI

    FDA Adverse Event
    SYNTHES (USA)·Product code NQP·July 3, 2008

    WATCHMAN FLX?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·April 15, 2026

    ISOLINE

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code MRM·August 25, 2015

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·May 19, 2017

    HANCOCK II MITRAL BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 9, 2019