BEUDAMED
    103 results · 29ms · Sources: EU EUDAMED, US FDA

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    SYNGO.CT VASCULAR ANALYSIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRINCETON

    FDA UDI
    Princeton Medical Group, Inc.·00810158212893·FORCEPS STANDARD TISSUE 1X2 TEETH 8"

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180188358·forceps tissue 1x2 teeth, 20cm

    DENALI

    FDA UDI
    ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042120242·Bracket Tweezer - Standard Large

    ZOLL Medical Corporation

    FDA registration
    ZOLL Medical Corporation·3 products·🇺🇸 United States

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981265700·Trial, 35mm x 27mm x 20mm, 20 deg

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981246464·Interbody, 35mm x 27mm X 20mm, 20 Deg

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321120200·

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0120200·Screwdriver, Modular Bone Screws

    POWERHEART G5 KIT,AUTO,BG-INTL EN

    FDA Adverse Event
    Malfunction ·CARDIAC SCIENCE CORPORATION·Product code MKJ·September 24, 2025

    BD PLASTIPAK¿ CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 13, 2022

    RESPIEVENTS SOFTWARE IS EVENT DATA PROCESSING SOFWARE FOR A PC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VEGA SPAN SPINOUS PROCESS PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2112020-1999-00004

    FDA Adverse Event
    Injury ·December 9, 1999

    POWERHEART G5 KIT,SEMI,KOR-INTL ENG

    FDA Adverse Event
    Malfunction ·CARDIAC SCIENCE CORPORATION·Product code MKJ·August 11, 2023

    G3 PLUS AUTO, AED, AHA 2010, US ENGLISH

    FDA Adverse Event
    Malfunction ·CARDIAC SCIENCE CORPORATION·Product code MKJ·February 7, 2020

    HNM Medical

    FDA UDI
    HNM STAINLESS, LLC.·00842962110607·MATHIU HEANEY NEEDLE HOLDER

    POWERHEART G5 KIT,SEMI,US EN/FRN CA, CPR

    FDA Adverse Event
    Death ·CARDIAC SCIENCE CORPORATION·Product code MKJ·December 9, 2024

    POWERHEART G5 KIT,SEMI,US EN/FRN CA, CPR

    FDA Adverse Event
    Death ·CARDIAC SCIENCE CORPORATION·Product code MKJ·December 9, 2024

    G3, AHA 2005, US ENGLISH, NB2S

    FDA Adverse Event
    Malfunction ·CARDIAC SCIENCE CORPORATION·Product code MKJ·October 1, 2021