BEUDAMED
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    Neeva Baby

    FDA UDI
    Sebe Inc·00860005571901·The Neeva Baby Fetal Doppler is an ultrasonic D...

    Neeva Baby

    FDA UDI
    Sebe Inc·00860005571925·The Neeva Baby Fetal Doppler Mini is an ultraso...

    Neeva Baby

    FDA UDI
    Sebe Inc·00860005571932·The Neeva Baby Fetal Doppler is an ultrasonic D...

    Neeva Baby

    FDA UDI
    Sebe Inc·00860005571987·Neeva Baby Heart Monitor

    SBE MEDICAL INC.

    FDA registration
    SBE MEDICAL INC.·1 product·🇺🇸 United States

    DRAPER PRODUCTS, INC./R. SABEE CO. LLC

    FDA registration
    DRAPER PRODUCTS, INC./R. SABEE CO. LLC·1 product·🇺🇸 United States

    UNKNOWN GRAFT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC WAYNE·Product code DYF·October 21, 2005

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·September 1, 2022

    OEC 8800

    FDA Adverse Event
    Malfunction ·GE BE MEDICAL SYSTEMS INC.·Product code JAA·January 27, 2010

    OEC STENOSCOPE

    FDA Adverse Event
    Malfunction ·GE BE MEDICAL SYSTEMS INC.·Product code JAA·February 16, 2010

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·April 12, 2021

    EPROM and Control Software (embedded), version 5.08, for the GammaMed 12i/t Afterloader, manufactured by Varian Medical Systems, Inc, Palo Alto, CA 94304.

    FDA Recall
    Terminated ·Varian Medical Systems·Product code JAQ·February 6, 2004

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·January 25, 2023

    DA VINCI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·April 29, 2025

    8800

    FDA Adverse Event
    Malfunction ·GE BE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 31, 2008

    GE OEC 8800

    FDA Adverse Event
    Malfunction ·GE BE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 12, 2008

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 7, 2018

    Medtronic Intersept 3608 Sterile tubing (8') 1/2 x 3/32 in. Quantity 10, Lot 7626621, Use by 2009-07-31. Manufacturer: Medtronic, Inc. Minneapolis, MN 55432-5604 USA. Different components and tubing sets are included within the Custom Pack depending on customer requirements. Tubing sets are placed within a plastic tray, which then is wrapped and placed inside a header bag and sealed at the plastic side. This bag seves as the product sterile barrier.

    FDA Recall
    Terminated ·Medtronic Perfusion Systems·Product code DWE·August 1, 2007

    640G INSULIN PUMP MMT-1711K

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·April 25, 2019

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·June 9, 2023