BEUDAMED
    682 results · 23ms · Sources: EU EUDAMED, US FDA

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    FILIFORM STRAIGHT TIP

    FDA Adverse Event
    Malfunction ·RUSCH INC.·Product code FBW·March 29, 2004

    FLIFORM WITH SPIRAL TIP

    FDA Adverse Event
    Injury ·RUSCH, INC.·Product code FBW·July 25, 1996

    INMED

    FDA Adverse Event
    Injury ·INMED CORP.·Product code FBW·July 29, 1996

    PORGES NEOPLEX

    FDA Adverse Event
    Injury ·MENTOR-PORGES·Product code FBW·March 17, 2004

    PHILIPS FOLLOWER - FILIFORM CATHETER

    FDA Adverse Event
    Injury ·INMED CORP.·Product code FBW·April 2, 1996

    PORGES BOUGIE FILIFORM/FOLLOWER

    FDA Adverse Event
    Malfunction ·PORGES S.A.·Product code FBW·April 21, 2000

    INTEGRAL FILIFORM URETHRAL DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FBW·August 9, 2024

    UNKNOWN DILATION PRODUCTS

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 4, 2026

    UNKNOWN DILATION PRODUCTS

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·April 29, 2026

    UNKNOWN DILATION PRODUCTS

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·April 30, 2026

    UNKNOWN DILATION PRODUCTS

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 3, 2026

    UNKNOWN DILATION PRODUCT

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 3, 2026

    UNKNOWN DILATION PRODUCT

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 1, 2026

    UNKNOWN DILATION PRODUCT

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 1, 2026

    UNKNOWN DILATION PRODUCTS

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 1, 2026

    UNKNOWN DILATION PRODUCT

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 3, 2026

    UNKNOWN DILATION PRODUCTS

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code FBW·May 1, 2026

    HEYMAN FOLLOWER, COUDE TIP, 20 FR

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·October 4, 2018

    BARD® HEYMAN FOLLOWER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·October 2, 2018

    HEYMAN FOLLOWER, COUDE TIP, 22 FR

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FBW·October 4, 2018