BEUDAMED
    14 results · 18ms · Sources: EU EUDAMED, US FDA

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    GISH RELIANCE OXYGENATOR (MODEL HFO)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239413·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 3 10mm ...

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108147·CASTROVIEJO NEEDLE HOLDER DELICATE CVD

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C1029615300·Cross Connector

    PREFERENCE

    FDA UDI
    CTL Medical Corporation·00841732151116·Cross-connector 30mm Fixed

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555102961530·30mm Fixed Cross Connector Assembly

    Bluetooth blood pressure monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MD-TEMP

    FDA 510(k)
    FDA Class 2 ·Dental

    IMPELLA CP

    FDA Adverse Event
    Death ·ABIOMED, INC.·Product code OZD·November 10, 2025

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 24, 2021

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code LZH·January 17, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 28, 2014

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·January 14, 2011

    ANTIROTSCR F/FEM NECK SYST F/CONSTRUCT L

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·October 23, 2019