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

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    OPTI-AMP DC-POWERED

    FDA 510(k)
    FDA Class 2 ·Neurology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704283488·KLEINERT-KUTZ HOOK 6" 3 MILLIMETER

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809849332·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE SMALL BL...

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981173821·L Con, Side-Loading, R, 16mm, 60mm

    EXPLANT™

    FDA UDI
    ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024311893·

    NATURAL ORDINARY RIBBED,DOTTED,AND CONTOURED (MALE RUBBER LATEX CONDOM, LUBRICATED W/SILICONE OIL

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MODIFICATION TO:HU-FRIEDY BRAND SATIN SWIVEL ULTRASONIC INSERT

    FDA 510(k)
    FDA Class 2 ·Dental

    ARCHITECT CA19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·October 31, 2025

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 19, 2026

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 11, 2013

    5 FR DL POWERPICC SOLO WITH TLS, MAXIMAL BARRIER PRECAUTION

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·March 1, 2011

    PRECISION XTRA / OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·May 20, 2008

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 1, 2026

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·December 4, 2017

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 14, 2026

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·December 9, 2025

    ARCHITECT CA19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·December 22, 2025

    ARCHITECT CA19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·April 3, 2026

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·June 11, 2021

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·May 28, 2022