BEUDAMED
    32 results · 24ms · Sources: EU EUDAMED, US FDA

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    OssGuide

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772412495·PROTECT.LUMBOSTYLE BACK SUPP BLACK III

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00142006230·CC-203

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034623·CFx Two

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471159064·T Ultra T° D-Form D 018X025

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034630·CFx Two, Base

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034647·CFx Two, Lid

    SCANDINAVIAN IVF SCIENCES AB, FREEZE-KIT 1

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DUOPRO SAFETY SYRINGE (DUOPROSS)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

    RETROFLEX 3 INTRODUCER SHEATH SET

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYB·July 1, 2013

    UNK HIP FEMORAL STEM SROM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 21, 2022

    UNK HIP FEMORAL SLEEVE SROM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 21, 2022

    BD PLASTIPAK 50ML CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 14, 2021

    UNK HIP FEMORAL STEM SROM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 21, 2022

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 21, 2022

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 21, 2022

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·September 15, 2022

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL.·Product code DTZ·March 12, 2024