BEUDAMED
    24 results · 19ms · Sources: EU EUDAMED, US FDA

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    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772344116·PROTECT.PRO ACTION BACK SUPPORT BLACK M

    Callaly Tampliner

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019149·1.2mm Fully Threaded Screw Drill Guide

    GYMK-20100/3

    Device
    EU MDR · Eu Md Class 1 ·AGA Sanitätsartikel GmbH·On the market·32 countries

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869611794·MOSS VRS rod rotation key

    Safecheck Gusseted Sterilization Reel(KR20100-3)

    Device
    EU MDR · Eu Md Class 1 ·Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.·On the market

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523130306·Knee Instrument Case 3 Base

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523130313·Knee Instrument Case 3 Tray

    Howmedica, Mix-Kit

    FDA UDI
    STRYKER CORPORATION·04546540257802·I Disposable Mixing Bowl and Spatula

    Z-NET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RAPIDVIT BLAST, RAPIDWARM BLAST

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

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·October 29, 2018

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    M2A-MAGNUM MOD HD SZ 42MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 2, 2013

    RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, MODEL #'S 1003006-20, 1003007-20, 1003008-20, 1003009-20, 1003010-20, 1003

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSE MANUFACTURING·Product code FKX·August 19, 2011

    QUIDEL QUICK VUE OTC COVID 19 TEST

    FDA Adverse Event
    Malfunction ·QUIDEL CORP.·Product code QKP·January 17, 2024

    QUIDEL QUICK VUE OTC COVID 19 TEST

    FDA Adverse Event
    Malfunction ·QUIDEL CORP.·Product code QKP·January 17, 2024

    Quanta System Sterile Optical Laser Fiber, reusable

    FDA Enforcement
    Class II ·Terminated·Quanta System, S.p.A.·June 16, 2021