BEUDAMED
    22 results · 37ms · Sources: EU EUDAMED, US FDA

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    ZIMMER DENTAL TAPERED SCREW-VENT M IMPLANT

    FDA 510(k)
    FDA Class 2 ·Dental

    IMP,TSV,MCOL MG,4.7MM,10M

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·May 21, 2024

    IMP,TSV,MCOL MG,4.7MM,11.5MML

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·May 21, 2024

    IMP,TSV,MCOL MG,4.7MM,11.5MML

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·June 12, 2024

    IMP,TSV,MCOL MG,3.7MM,11.5MML

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·July 23, 2024

    IMP,TSV,MCOL MG,4.7MM,11.5MML

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 1, 2023

    IMP,TSV,MCOL MG,4.7MM,11.5MML

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·June 16, 2022

    IMP,TSV,MCOL MG,4.7MM,10M

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·September 9, 2025

    IMP,TSV,MCOL MG,4.7MM,11.5MML

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·December 27, 2024

    IMP,TSV,MCOL MG,4.7MM,13M

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·July 20, 2023

    IMP,TSV,MCOL MG,4.7MM,10M

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·February 13, 2019

    Flexitron

    FDA UDI
    Nucletron B.V.·08717213027282·Flexitron Transfer Tube for 4F Flexibles (36)

    ULTRA -THIN SDS BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DECOMPRESSION OF CHOICE AND NEURO DECOMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQY·December 8, 2006

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/10 MM L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 7, 2022

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·May 14, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 2, 2011

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·August 12, 2008

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012