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

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    CLEARFIL ST OPAQUER

    FDA 510(k)
    FDA Class 2 ·Dental

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·00304040151525·ZIRLUX ACETAL MILLING DISC

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010080592·CURRETTE OPEN 4MM

    Innomed, Inc.

    FDA UDI
    INNOMED, INC.·00840277114723·Screw Removal System Extractor Wrench

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033449714·

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033449738·

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033449721·

    SOFIA VERGARA

    FDA UDI
    FGX INTERNATIONAL INC.·00193033449691·

    KSEA MINIATURE NEUROENDOSCOPE

    FDA 510(k)
    FDA Class 2 ·Neurology

    DORNIR LC-1 CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INSET 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 6, 2025

    PORTEX 7.0MM SUCTIONAID TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL LTD·Product code CAZ·February 22, 2013

    TERUMO VIRTUOSAPH VEIN HARVESTING SYSTEM

    FDA Adverse Event
    TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·February 28, 2011

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·March 12, 2008

    STENT - VASCULAR RECONSTRUCTION

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·December 12, 2017

    STENT - VASCULAR RECONSTRUCTION

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·December 12, 2017

    STENT - VASCULAR RECONSTRUCTION

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·December 12, 2017

    STENT - VASCULAR RECONSTRUCTION

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·December 12, 2017

    Zimmer brand Knowles pin with 5/32 in. threaded diameter, 1/8 in. shaft diameter and 6 inches in length. Catalog # 281-01-15.

    FDA Recall
    Terminated ·Zimmer Inc·Product code JDW·October 15, 2003

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012