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    MN Health, Inc

    FDA registration
    MN Health, Inc·9 products·🇺🇸 United States

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425139·EcoPression VPS Putty Kit Base & Catalyst - Reg...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425108·EcoPression VPS Medium Body Impression Material...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425146·EcoPression VPS Putty Kit Base & Catalyst - Fas...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425092·EcoPression VPS Medium Body Impression Material...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425115·EcoPression Bite Registration Material – Fast S...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425993·EcoPression VPS Heavy Body Impression Material ...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425061·EcoPression VPS Heavy Body Impression Material ...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425085·EcoPression VPS Light Body Impression Material ...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425122·EcoPression Bite Registration Material – Super ...

    EcoPression

    FDA UDI
    MN Health, Inc.·00850072425078·EcoPression VPS Light Body Impression Material ...

    RMH3 Dental

    FDA UDI
    MN Health, Inc.·00850072425245·Tartar, Stain & Permanent cement remover Liquid...

    VISIONAIRE 5

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code CAW·March 2, 2023

    TEMPORARY PACING LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code LDF·October 13, 2023

    LIAISON® XL MUREX HCV AB

    FDA Adverse Event
    Malfunction ·DIASORIN S.P.A UK BRANCH·Product code MZO·January 13, 2023

    HEARTWARE VENTRICULAR ASSIST SYSTEM-CONTROLLER 2.0

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·March 16, 2018

    CADD-MS 3 Ambulatory Infusion Pump, Model 7400 Smiths Medical MD, Inc., St. Paul, MN 55112 USA. Electromechanical pumps used for general drug delivery infusion therapies. Used mainly by home care patients but can also used in health care facilities.

    FDA Recall
    Terminated ·Smiths Medical MD, Inc.·Product code FRN·March 7, 2008

    ETHICON brand surgical device with an added label with the labeling Manufactured by: MedSurg Solutions, 3025 Harbor Lane suite 104 Plymouth, MN 55447 and/or another additional label which states MEDSURG 3025 Harbor Lane, Suite 104, Plymouth, MN 55447 Steriliation Date:. The product labels also state the following firm: ETHICON, INC. SOMERVILLE, N.J. 08876-0151 The product described on label is a ''Stapler, reload, TR35W, TR776, TCR 75, TCR 55, TRT75,

    FDA Recall
    Terminated ·International Surgical Supply, Inc.·Product code KDC·September 3, 2003

    ETHICON brand surgical device with an added label with the labeling Manufactured by: MedSurg Solutions, 3025 Harbor Lane suite 104 Plymouth, MN 55447 and/or another additional label which states MEDSURG 3025 Harbor Lane, Suite 104, Plymouth, MN 55447 Steriliation Date:. The product labels also state the following firm: ETHICON, INC. SOMERVILLE, N.J. 08876-0151 The product described on label is a: Stapler EMS Endo Hernia , item # 8034.

    FDA Recall
    Terminated ·International Surgical Supply, Inc.·Product code KDC·September 3, 2003

    ETHICON brand surgical device with an added label with the labeling Manufactured by: MedSurg Solutions, 3025 Harbor Lane suite 104 Plymouth, MN 55447 and/or another additional label which states MEDSURG 3025 Harbor Lane, Suite 104, Plymouth, MN 55447 Steriliation Date:. The product labels also state the following firm: ETHICON, INC. SOMERVILLE, N.J. 08876-0151 The product described on label is a: Thoracic Trocar Sleeve, rounded tip, Item # TT012.

    FDA Recall
    Terminated ·International Surgical Supply, Inc.·Product code KDC·September 3, 2003