BEUDAMED
    22 results · 26ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04046114938231·GENUMEDI PRO ROM SIZE III

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377068156·RELINE C Conn,3.5-4/5-6mm Clsd In-Line

    Peerless Buccal Tube

    FDA UDI
    ORMCO CORPORATION·00889989022605·PEERLESS 0DEG SGLLFM-22TRQX022 LR

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746099755·DB BKT MASTER 4.5MM LEWIS LOWER ANT 018 T-5 A=0...

    Enema Kit: Empty Enema Bag Delivery System

    FDA UDI
    Bracco Diagnostics Inc.·10815112020634·Empty Snap Cap Bag

    Enema Kit: Empty Enema Bag Delivery System

    FDA UDI
    Bracco Diagnostics Inc.·10815112021587·Empty Snap Cap Bag

    Enema Kit: Empty Enema Bag Delivery System

    FDA UDI
    Bracco Diagnostics Inc.·10815112020825·Empty Snap Cap Bag

    MyndMove

    FDA UDI
    MyndTec Inc·00692520003038·

    MyndMove

    FDA UDI
    MyndTec Inc·06925209003031·

    AcQCross Qx

    FDA UDI
    ACUTUS MEDICAL, INC.·00850027837123·AcQCross Qx - VZ 71cm

    FlexCath Cross Transseptal Solution

    FDA UDI
    ACUTUS MEDICAL, INC.·00850027837802·FlexCath Cross Transseptal Solution– VZ 71 cm

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756018685·SHOULDER IMMOBILIZER

    Mariner

    FDA UDI
    Seaspine Orthopedics Corporation·10889981129453·Set Screw Starter, T-Handle, Short

    XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEALTHCARE SERVICE AND SUPPLY ALP ALTERNATING LEG PRESSURE PUMP AND GARMENTS FOR THE LIMB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AFFERA

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code QZI·May 7, 2026

    HUMERAL STEM #H6 RIGHT

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JDB·August 29, 2022

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·May 6, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·January 7, 2013