BEUDAMED
    21 results · 24ms · Sources: EU EUDAMED, US FDA

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    BD PROBE TEC URINE PRESERVATIVE TRANSPORT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809849554·FOR MEN 15-20 MM HG KNEE HIGH CLOSED TOE LARGE ...

    Oph.Forceps

    FDA UDI
    KATENA PRODUCTS, INC.·00841668116081·Colibri Fcps, Pierse W/Plat, Titanium

    SINGLE ACTION BIOPSY NEEDLE, MODEL RCBS: XX GAUGE, XX LENGTH, XX THROW

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

    XPS 3000 SYSTEM

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

    IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·November 15, 2015

    BOM 7MM EXTENDED LENGTH ENDOSCOPE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GCJ·March 27, 2019

    BASEPLATE IMPACTOR, ASSEMBLY

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 1, 2024

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 8, 2019

    AVL ANGLED REAMER SLEEVE ASSEMBLY, 15

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·April 29, 2024

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·March 13, 2024

    AVL ANGLED REAMER SLEEVE ASSEMBLY, 25

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·March 21, 2024

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 4, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·September 2, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·April 12, 2011

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 13, 2019

    UNIVERS REVERS APEX IMPACTOR/EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·January 7, 2025

    MICRODEBRIDER 1898200T IGS M4

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·May 15, 2014

    Scorpio Total Knee Posteriorly Stabilized Femoral Component, #7R, Catalog No.: 71-4107R, Lot Code: K05L310; Scorpio Total Knee Posteriorly Stabilized Femoral Component, #7L, Catalog No. 71-4506L, Lot Code K05L224.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code KWY·November 8, 2005

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 15, 2019