BEUDAMED
    23 results · 31ms · Sources: EU EUDAMED, US FDA

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    U-TEX

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517702012·BASE Trial, 8x38x28mm 10°

    VENTRALIGHT

    FDA UDI
    Davol Inc.·00801741031786·Ventralight ST Mesh with Echo PS Positioning Sy...

    Zuma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981097424·Modular Bullet Paddle Distractor 10mm

    MER BAG

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NOILES(TM) TOTAL KNEE PROSTHESIS, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·July 17, 2024

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026

    BI-METRIC/X POR NC 11X135

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 13, 2018

    M2A 38MMX50MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    BP ADVANCED PERSONAL DOUBLE

    FDA Adverse Event
    Malfunction ·MEDELA, INC.·Product code HGX·June 25, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 11, 2013

    TENDRIL SDX

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

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026

    M2A 38MM MOD HD+9MM NK NO SKRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    Bard¿ Ventralight" ST Mesh with Echo PS" 8"x10" Reorder Number: 5955810 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

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025

    VENTRALIGHT ST W/ ECHO

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

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018