BEUDAMED
    53 results · 116ms · Sources: EU EUDAMED, US FDA

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    OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Sammons Preston

    FDA UDI
    Performance Health Supply, LLC·00885914108079·Sammons Preston Refillable Ice Bag w/Clamp Clos...

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033863·Baltic Denture System BDLoad BDLoad ↓ Lm6 PLSEu...

    AUTOMED 3000 INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CRYSTAL MONITOR MODEL 16

    FDA 510(k)
    FDA Class 2 ·Neurology

    OPTETRAK

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 2, 2022

    LOGIC TIBIA PS MOD INSRT SZ 3 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 2, 2022

    LOGIC TIBIA PS MOD INSRT SZ 5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 23, 2022

    SYNCARDIA CARDIOWEST

    FDA Adverse Event
    Injury ·SYNCARDIA SYSTEMS, INC.·Product code DSQ·April 3, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·March 17, 2011

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·April 24, 2008

    OPTETRAK

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 4, 2022

    LOGIC TIBIA PS MOD INSRT SZ 4 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 3, 2024

    NO CODE AVAILABLE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code GXN·March 8, 2016

    TIBIAL COMPONENT PRECOAT RIGHT MEDIAL/LEFT LATERAL SIZE 3

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HSX·February 3, 2017

    LOGIC TIBIA PS MOD INSRT SZ 5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 10, 2023

    LOGIC TIBIA PS MOD INSRT SZ 5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 10, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 11, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 6, 2025

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 11, 2024