BEUDAMED
    26 results · 30ms · Sources: EU EUDAMED, US FDA

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    DOLOMITE Anterior Cervical Stabilization System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112496·BARRON VACUUM TREPHINE 7.5MM

    SprintRay High Impact Denture Teeth - Bleach

    FDA UDI
    Sprintray, Inc.·00850039704291·SprintRay High Impact Denture Teeth is a light-...

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112489·BARRON VACUUM TREPHINE 7.25MM

    VICEROY Spinal System

    FDA UDI
    EOS BIOTEK,INC.·88000163012122·

    Viceroy

    FDA UDI
    DIOMEDICAL CO.,LTD.·08800039826303·Rod Pre-Bent 6.0 x 65mm

    PATIENT LATEX POLYMER COATED POWDER-FREE GLOVES, CONTAINS 50 MICROGRAM OR LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER GR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·January 10, 2024

    NELLCOR N-550 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code DQA·October 15, 2008

    IMPRESS DIAGNOSTIC PERIPHERAL CATHETER

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·June 27, 2013

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·August 11, 2011

    Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic

    FDA Recall
    Terminated ·Surgical Instrument Service And Savings, Inc.·Product code HRH·May 3, 2013

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 23, 2022

    BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 2, 2024

    Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic

    FDA Enforcement
    Class II ·Terminated·Surgical Instrument Service And Savings, Inc.·July 10, 2013

    ENDURANT BIFURCATED STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·June 17, 2020

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·October 9, 2021

    VALIANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·July 21, 2021

    BD VACUTAINER MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 23, 2020