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

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    Contact Lens Case (multiple brand name)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694009164·2.3mm Cannulated Drill, Manual

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022613·KLEOS PSL METAL MBT 022 UL1 PK5

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481124204·LOCATOR F-Tx Abutment for Mini Platform GS Conn...

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481123139·LOCATOR R-Tx Attachment System for TS/ET Fixtur...

    TMA - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989029635·ARCH TMA REV.CURVE LWR 019X025 PK/10

    NA

    FDA UDI
    STERILMED, INC.·10888551039338·DRILL BIT CANNULATED

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707016816·CALIBRA 1ST MOLAR BANDS n.LR 5

    Sorrento Bone Graft Substitute Strip (5cc)

    FDA UDI
    XENCO MEDICAL LLC·B064HB11600051·Sorrento Bone Graft Substitute Strip (5cc) 5cm ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694067782·Cannulated 2.3mm Drill, Manual Sterile Qty 2

    SYNCRO - BLUE TUBE, THE MAGNETICALLY GUIDED ENTERAL FEEDING TUBE- 8FR TUBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD PEN NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CI-1600-05

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS, LLC·Product code MCM·May 16, 2025

    CLEARLINK PACLITAXEL SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·February 2, 2024

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·June 10, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    GE OEC 8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 12, 2008

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 11, 2022

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 14, 2026

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 24, 2021