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

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    Filters Regulation: Us FDA ×

    SteriCap Mini Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304270466·

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193110752·HA PEEK EVOS Rotate, , 16mmx12mmx 30mm , FLAT 8...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528128176·3.0 X 16mm Cannulated Headed Screw, T10

    VERI-Q SELF-TESTING AND VERI-Q PLUS MGD-2001 BLOOD GLUCOSE MONITORING SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACTHYDERM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    I-STAT 6+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·May 22, 2019

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 3, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIM·June 21, 2013

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·April 5, 2023

    VANGUARD COMPLETE KNEE SYSTEM - CR TIBIAL BEARING 10X79/83

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 17, 2017

    DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·August 13, 2021

    DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·July 27, 2022

    COONS DILATOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DRE·July 28, 2022