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

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    RAPIDFLAP LS CRANIAL FLAP FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Spherodon +

    FDA UDI
    SILMET LTD·07290016787733·Dental Amalgam Capsules

    ArgenZ HT+ 98x12 ML OM1B

    FDA UDI
    ARGEN CORPORATION, THE·D818130309·Dental porcelain/ceramic restoration kit

    EVONOS

    FDA UDI
    Gyrus ACMI, LLC·00821925012677·SCHEER GELFOAM PLACER

    N/A

    FDA UDI
    Tyber Medical, LLC·M695M1303090·

    LINK Instruments - Forceps and clamps

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575344529·Orthopaedic joint/limb rongeur - Cemented Aceta...

    LINK Instruments - Forceps and clamps

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575344536·Orthopaedic joint/limb rongeur - Cemented Aceta...

    FOB ONE STEP RAPID TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    OSTEORAPTOR CURVED 2.3 SUTURE ANCHORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CONMED PENCIL 130309

    FDA Adverse Event
    CONMED ELECTROSURGERY·Product code GEI·October 19, 2006

    CONMED

    FDA Adverse Event
    Malfunction ·CONMED/ASPEN LABS·Product code GEI·June 26, 2000

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·December 29, 2025

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·May 24, 2013

    FREESTYLE LITE

    FDA Adverse Event
    Injury ·Product code NBW·June 16, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 22, 2008

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA - S.R.L.·Product code DTZ·February 19, 2026

    HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL VENOUS/CAR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 10, 2019

    INSPIRE 6F HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 10, 2017

    COMP LK SCR 3.5HEX 4.75X25 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·September 19, 2022

    INSPIRE 6F HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·August 3, 2022