BEUDAMED
    23 results · 19ms · Sources: EU EUDAMED, US FDA

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    ALP-KII

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SWANSON

    FDA UDI
    WRIGHT MEDICAL TECHNOLOGY, INC.·00840420190017·Finger Joint Sizer

    Stryker

    FDA UDI
    Provision·B504GS48100080·

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334012274·McCrea Female Sound, Curved. 3/4-inch nominal b...

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334001230·Bi-Terminal handle with cord, Bovie special plugs.

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K1100080·Tray Insert

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100080·Dilator Sleeve, Probe

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K1100080·Tray Insert

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100080·Tray Insert 1, Cosmolock, Arcamed

    GOLIFE NASAL MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AXXESS SPINAL CORD STIMULATION LEAD, MODEL 8000 SERIES, INCLUDING 80XX, 81XX, AND 82XX

    FDA 510(k)
    FDA Class 2 ·Neurology

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRASOL(TM)

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRASOL(TM)

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRASOL(TM)

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRASOL(TM)

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRASOL(TM)

    ZYNO MEDICAL ADMINISTRATION SET FOR Z-800 INFUSION PUMP SYSTEM

    FDA Adverse Event
    Malfunction ·ZYNO MEDICAL, LLC·Product code FPA·March 19, 2021

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 25, 2014

    HS ACE 23 CM SCISSOR HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code LFL·November 12, 2007

    DTL SET SCREW

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code NKB·October 23, 2012