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

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    AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Inspire™/Temptation® Now 76g Syringe Mixing Tips

    FDA UDI
    DEN-MAT HOLDINGS, LLC·00359883004026·Dental material mixing nozzle, non-sterile

    Inspire™/Temptation® Now 76g Syringe Mixing Tips

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002134·Dental material mixing nozzle, non-sterile

    Column, Ascarite Desiccator, Disposable

    FDA UDI
    A-M SYSTEMS, LLC·00817081026115·Column, Ascarite Desiccator, Disposable

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100271·SAUER INFANT SPECULUM

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111084058·SKLARCUT OP SCIS STR SS 5 1/2

    Malibu™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981030827·PRECONTOURED ESS PLUS ROD, 5.5 x 500 mm

    Monster® Screw System

    FDA UDI
    Paragon 28, Inc.·00889795035967·Countersink, 3.5 Headless

    GORE EMBOLIC FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FRAMELESS RADIOSURGERY COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Radiology

    MICRO 20G

    FDA UDI
    The Wells Johnson Company·B458201535000·Cannula, Micro 20g, on dll, specify length and ...

    II Ring Retractor

    FDA UDI
    Automated Medical Products Corp.·00810118341557·Horizontal Flex Bar 1”

    ESON 2 NASAL MASK

    FDA Adverse Event
    Injury ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·August 14, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 16, 2025

    MCGHAN 153 500 CC

    FDA Adverse Event
    Injury ·Product code FTR·January 18, 2011

    GMK-PRIMARY TIBIAL TRAY FIXED CEMENTED SIZE 5 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 20, 2019

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 8, 2013

    ELLIPSE DR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·October 8, 2014

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD.·Product code JAA·June 21, 2011

    SNORERX

    FDA Adverse Event
    Injury ·APNEA SCIENCES·Product code LRK·May 22, 2017