BEUDAMED
    21 results · 22ms · Sources: EU EUDAMED, US FDA

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    SHILEY CUFFED PEDIATRIC TRACHEOSTOMY TUBE; LONG CUFFED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VENTRALIGHT

    FDA UDI
    Davol Inc.·00801741031755·Ventralight ST Mesh with Echo PS Positioning Sy...

    AMERLITE PROCESSING CENTER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    543 SERIES BTE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C. R. BARD, INC.·Product code FTL·September 2, 2022

    VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·September 2, 2022

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·October 21, 2023

    VENTRALIGHT ST W/ECHO

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·January 25, 2017

    DEPUY ASR XL FEM IMP SIZE 39

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 11, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·July 24, 2014

    Bard¿ Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number: 5955680 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

    FDA Enforcement
    Class II ·Terminated·Davol, Inc., Subs. C. R. Bard, Inc.·June 11, 2014

    VENTRALIGHT ST W/ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·December 6, 2018

    VENTRALIGHT ST W/ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·December 6, 2018

    VENTRALIGHT ST W/ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·September 14, 2018

    VENTRALIGHT ST W/ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·June 1, 2018

    VANGUARD PS OPEN FEMORAL INTERLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 18, 2017

    BIOMET OFFSET TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 18, 2017

    Bard Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number: 5955680 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

    FDA Recall
    Terminated ·Davol, Inc., Subs. C. R. Bard, Inc.·Product code GCJ·April 24, 2014

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·October 14, 2020