BEUDAMED
    50 results · 28ms · Sources: EU EUDAMED, US FDA

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    SPECTRUM CENTRAL VENOUS CATHETER WITH OR WITHOUT HYDROPHILIC COATING

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033843·Baltic Denture System BDLoad BDLoad ↓ Sw6 PLSEu...

    NA

    FDA UDI
    NT-Trading GmbH & Co. KG·ENTTCAM60338431·Abutment Screw

    ENVIVE MINIFORMS

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    AUTOSET SPIRIT CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    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

    ABSORB BIORESORBABLE VASCULAR SCAFFOLD SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·April 3, 2013

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 17, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·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

    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

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 9, 2024

    LOGIC FEMORAL PS CEM RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 21, 2024