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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Gebauer’s Pain Ease Topical Anesthetic Skin Refrigerant (Mist Spray and Medium Spray)

    FDA 510(k)
    FDA Unclassified ·Unknown

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694027076·2.0mm X 28mm Cannulated Headless Screw

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023058·Male Post, 1 Hole

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068581·Cannulated 2.0 x 28mm Headless Screw Sterile Qty 5

    QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF MONODERM

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

    NEOTRACT ANCHOR SYSTEM MODEL TAS400

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

    MEDIVATOR ENDOGATOR IRRIGATION TUBING

    FDA Adverse Event
    Malfunction ·MEDIVATORS INC·Product code OCX·August 15, 2025

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    MEDIVATOR ENDOGATOR IRRIGATION TUBING

    FDA Adverse Event
    Malfunction ·MEDIVATOR, INC.·Product code OCX·August 15, 2025

    MEDIVATOR ENDOGATOR IRRIGATION TUBING

    FDA Adverse Event
    Malfunction ·MEDIVATOR, INC.·Product code OCX·August 15, 2025

    PCA IV TUBING

    FDA Adverse Event
    Injury ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·August 26, 2025

    HYDRATOME RX 44

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·June 5, 2025

    QUILL SRS

    FDA Adverse Event
    Malfunction ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·September 3, 2008

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·February 13, 2009

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER INTERNATIONAL INC.·Product code KDJ·October 22, 2024

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·September 18, 2008