BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    SALINE FOR IRRIGATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981209667·Trial, 9mm x 32mm x 13mm, 8 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194550·Interbody, 9mm x 32mm x 13mm, 8 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202545·Interbody, 9mm x 32mm x 13mm, 8 deg

    WaveForm TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981243715·Interbody, 9mm x 32mm x 13mm, 8 Deg, 3D

    RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MEDTRONIC SINGLE USE ESOPHAGEAL MANOMETRIC CATHETER, MEDTRONIC SINGLE USE ANORECTAL MANOMETRIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 18, 2013

    MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-CLONMEL·Product code MAF·December 17, 2010

    UNKNOWN_KIE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HWC·July 14, 2014

    SYMPHONY OCT SYSTEM AO HANDLE, MEDIUM WITH RATCHET

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code LXH·August 22, 2024