BEUDAMED
    316 results · 29ms · Sources: EU EUDAMED, US FDA

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    Gambro UF Solutions Inc

    Manufacturer
    🇺🇸 United States

    Gambro Renal Products, Inc.

    Manufacturer
    🇺🇸 United States

    POLYFLUX REVACLEAR

    FDA UDI
    GAMBRO RENAL PRODUCTS, INC.·07332414101695·Revaclear-Revaclear Max are indicated for the t...

    REVACLEAR

    FDA UDI
    GAMBRO RENAL PRODUCTS, INC.·07332414123055·Revaclear 300 and 400 dialyzers are indicated f...

    Dual Lumen Extended Length Catheter and GALT insertion kit

    FDA UDI
    GAMBRO UF SOLUTIONS, INC·07332414119324·The Aquadex System is indicated for temporary (...

    Blood Circuit Set

    FDA UDI
    GAMBRO UF SOLUTIONS, INC·07332414112387·The Aquadex System is indicated for temporary (...

    Blood Circuit Set

    FDA UDI
    GAMBRO UF SOLUTIONS, INC·07332414112370·The Aquadex System is indicated for temporary (...

    Dual Lumen Extended Length Catheter

    FDA UDI
    GAMBRO UF SOLUTIONS, INC·07332414112363·The Aquadex System is indicated for temporary (...

    Aquadex FlexFlow

    FDA UDI
    GAMBRO UF SOLUTIONS, INC·07332414112301·The Aquadex System is indicated for temporary (...

    POLYFLUX REVACLEAR MAX

    FDA UDI
    GAMBRO RENAL PRODUCTS, INC.·07332414101701·Revaclear-Revaclear Max are indicated for the t...

    AUTO EFFLUENT SET

    FDA UDI
    GAMBRO UF SOLUTIONS, INC·07332414118914·The Auto Effluent Accessory is indicated for us...

    REVACLEAR

    FDA UDI
    GAMBRO RENAL PRODUCTS, INC.·07332414124076·Revaclear 400 dialyzer is indicated for treatme...

    NA

    FDA UDI
    GAMBRO UF SOLUTIONS, INC·07332414112264·A6001 5L Effluent Bag

    GAMBRO DIALYSIS MACHINE

    FDA Adverse Event
    Malfunction ·GAMBRO, INC.·Product code FII·September 27, 2000

    GAMBRO

    FDA Adverse Event
    Malfunction ·GAMBRO, INC.·Product code FII·September 27, 2000

    PHOENIX

    FDA Adverse Event
    Injury ·GAMBRO INC.·Product code FII·September 9, 2004

    PHOENIX

    FDA Adverse Event
    Injury ·GAMBRO INC.·Product code KDI·August 19, 2004

    PHOENIX

    FDA Adverse Event
    Injury ·GAMBRO INC.·Product code FII·August 31, 2004

    PHOENIX

    FDA Adverse Event
    Injury ·GAMBRO, INC.·Product code KDI·September 24, 2004

    PRISMA

    FDA Adverse Event
    Malfunction ·GAMBRO, INC.·Product code KDI·December 5, 2005