BEUDAMED
    785 results · 27ms · Sources: EU EUDAMED, US FDA

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    Reprocessed NRG Transseptal Needle

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mays

    FDA UDI
    Preat Corporation·00842092110577·Mays Unilateral Attach UR/LL

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694005876·MINCRO Screw Organizer Block

    Drill Guide

    FDA UDI
    Treace Medical Concepts, Inc.·00810111221511·Staple Drill Guide

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694010900·1.2mm Screw Depth Gauge

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2522000600·Straight Titanium Rod

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840967195377·SILICONE HANDLE, LARGE T, INT. 1/4" SQ., TORQUE...

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555252200060·Taurus Pedicle Screw System- Straight Rod 5.5x60mm

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555102200060·Straight Rod 6.0mm, 60mm

    GEL MARK BIOPSY SITE MARKER, MODELS MKOOO1, MK0004, MK0007

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ASTOFLO

    FDA 510(k)
    FDA Class 2 ·Hematology

    MEDTRONIC PLATE 7200060

    FDA Adverse Event
    Injury ·MEDTRONIC ENGINEERING AND INNOVATION CENTER (MEIC)·Product code KWQ·October 16, 2023

    Zimmer Trilogy Acetabular System Shell with Cluster Holes, Porous, 60mm O.D., Tivanium TI-6AL-4V Alloy, Hip Prosthesis Component, REF 6200-060-22, Catalog # 00-6200-060-22, Zimmer, Inc., Warsaw, IN, 46580.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code LPH·October 19, 2007

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 15, 2008

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 10, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 1, 2013

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021