BEUDAMED
    39 results · 29ms · Sources: EU EUDAMED, US FDA

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    V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bur PM2-95 80K Diamond Ø2.0 sterile

    FDA UDI
    Bien-Air Surgery SA·17630055515398·

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193107967·HA PEEK EVOS Straight, ,12mmx8mmx 26mm , FLAT ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694025898·3 x 2 Hole Left L Plate

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694098052·Sterilization Container, 2 BPS

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR21010121·Roncone PDS .020"x.020" Ultra Thermal Upper

    Biliary Drainage Tube

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170046476·

    DIGITAL INTEGRATION SYSTEM, DIS2000

    FDA 510(k)
    FDA Class 2 ·Radiology

    POWDER FREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MOSAIC MITRAL BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·August 2, 2019

    CG FUTURE BAND

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 15, 2018

    ACCELERATOR A3600

    FDA Adverse Event
    Malfunction ·INPECO SA·Product code JQP·December 20, 2024

    DELTA CER HEAD 12/14 32MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LZO·September 8, 2021

    ALTRX NEUT 32IDX50OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 8, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 19, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 24, 2011

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·June 10, 2021

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 26, 2021

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·May 16, 2023