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

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    Filters Regulation: Us FDA ×

    Empulse M90

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CETYLITE INDUSTRIES, INC.

    FDA registration
    CETYLITE INDUSTRIES, INC.·3 products·🇺🇸 United States

    smARTrack Feeding Tube System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Invictus™ OsseoScrew® System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EZTETIC DENTAL IMPLANT, 3.1MM DIAMETER, 2.9MMD PLATFORM, 11.5MM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 18, 2024

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 2, 2023

    SL 1 INTRODUCER UNK

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DYB·March 10, 2011

    RESPONSE EP CATHETER UNK

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DRF·March 10, 2011

    TRANSSEPTAL NEEDLE, BRK SERIES

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·March 10, 2011

    UNK

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·November 20, 2008

    ACCESS® 2 IMMUNOASSAY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 10, 2011

    GYNECARE MORCELLEX TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code HET·July 23, 2013

    EZTETIC DENTAL IMPLANT, 3.1MM DIAMETER, 2.9MMD PLATFORM, 11.5MM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·September 21, 2021