BEUDAMED
    192 results · 21ms · Sources: EU EUDAMED, US FDA

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    Lens, Contact, Orthokeratology, Overnight

    FDA Pre-Market Approval
    FDA Class 3 ·Optimum Infinite (tisilfocon A) Orthokeratology Lenses II

    M-TWO INSTRUMENT

    FDA UDI
    SWEDEN & MARTINA SPA·D7700457693·M-TWO INSTRUMENT 40/.04 25 MM, 6 PCS

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00887517441034·Universal Bender, Cross Connector Right

    LCP

    FDA UDI
    Synthes GmbH·10886982164612·4.5MM LCP PROXIMAL TIBIA PLATE 12 HOLES/226MM-LEFT

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361023319·Ø8MM FUSION SCREW, GEN II, SACROFUSE, 45MM

    Monster Screw System

    FDA UDI
    Paragon 28, Inc.·00889795001191·Flat Washer for Monster Screw 4.5mm

    Monster Screw System

    FDA UDI
    Paragon 28, Inc.·00889795001184·Dome Washer for Monster Screw 4.5mm

    QStat Cartridge

    FDA 510(k)
    FDA Class 2 ·Hematology

    RELAY PRO THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·November 23, 2021

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·September 30, 2024

    CUSTOM-MADE RELAY PRO NBS THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Injury ·BOLTON MEDICAL, INC.·Product code MIH·February 6, 2025

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·August 22, 2024

    CELL-DYN WBC REAGENT A

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·November 24, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 8, 2011

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·July 11, 2013

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·RelayPro Thoracic Stent-Graft System

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (SENOFILCON A) CONTACT LENS, CLEAR AND VISIBILITY TINTED WITH UV BLOCKER

    RELAY PRO THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·July 15, 2021

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (SENOFILCON A) CONTACT LENSES

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (senoflicon A) Brand Contact Lenses