BEUDAMED
    45 results · 20ms · Sources: EU EUDAMED, US FDA

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    JETYO

    FDA registration
    JETYO·1 product·🇹🇼 Taiwan

    Sunset

    FDA UDI
    Jetro Holdings, LLC·00760695034901·sunset x lg nitrile black powder free exam gloves

    Sunset

    FDA UDI
    Jetro Holdings, LLC·00760695334919·nitrile powder free exam gloves black medium

    sunset

    FDA UDI
    Jetro Holdings, LLC·00760695034895·sunset black nitrile exam gloves powder free large

    GYNECARE

    FDA Adverse Event
    Malfunction ·GYNECARE JETCO·Product code MNB·June 15, 2005

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·March 21, 2003

    CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL BIOPROSTHESIS.

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·January 18, 2002

    CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·July 3, 2008

    FREESTYLE BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES·Product code LWR·July 29, 2005

    TRANSSEPTAL NEEDLE, BRK SERIES, ADULT 18 GA, 98CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·July 11, 2011

    SIMUPLUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code KRH·July 23, 2025

    AGILIS NXT, 8.5F, STEERABLE INTRODUCER, MED CURL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DYB·July 11, 2011

    Quick Connect component p/n 201048. The component is contained in QPC1713 and QPC1724 Quick Connects. The QPC1724 is used to attach Pentax 70/70K/72/72K/80K/81K/90i/90K SERIES GI ENDOSCOPES WITH WATER JET to the C1160 Universal Flexible Processing Tray in the SYSTEM 1 Sterile Processing System. The QPC1713 is used to attach Pentax 70/70K/80K/85/85K/90K SERIES GI ENDOSCOPES without WATER JET to the C1160 Universal Flexible Processing Tray in the SYSTEM 1 Sterile Processing System.

    FDA Recall
    Terminated ·Steris Corp·Product code MED·August 4, 2008

    HUDSON NEBULIZER W/ADULT MASK & TBG, SMALL VOL

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCQ·July 31, 2015

    EDWARDS INSPIRIS RESILIA AORTIC VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·October 13, 2021

    BUNNELL

    FDA Adverse Event
    Malfunction ·BUNNELL, INC.·Product code LSZ·September 12, 2014

    ST. JUDE MEDICAL EPIC VALVE MITRAL VALVE 25MM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL / ABBOTT MEDICAL·Product code LWR·August 4, 2023

    TRIFECTA VALVE WITH GLIDE TECHNOLOGY AORTIC VALVE 21MM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL / ABBOTT MEDICAL·Product code LWR·August 4, 2023

    HUDSON UP-DRAFT II OPTI-NEB NEBULIZER W/7 FT

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·May 24, 2017

    MITRACLIP G4 CLIP DELIVERY SYSTEM (MDD)

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NKM·May 7, 2024