BEUDAMED
    22 results · 23ms · Sources: EU EUDAMED, US FDA

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    Inclusive Titanium Abutments compatible with: MegaGen AnyRidge Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    Surgidac

    FDA UDI
    Covidien LP·20884521127019·Polyester Triple Stitch Reload

    STAINLESS STEEL FEMORAL NAILING SYSTEM

    FDA UDI
    ORTHOFIX SRL·18053504365730·Component. Not for sale. Used for reporting Dir...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197065627·GUTHRIE Skin Hook 2.5mm wide 130mm,...

    ENDO STITCH

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code OCW·December 22, 2022

    ENDO STITCH

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code OCW·December 22, 2022

    ENDO STITCH

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code OCW·December 22, 2022

    SURGIDAC

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code OCW·December 22, 2022

    SURGIDAC

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code OCW·December 22, 2022

    FIREBIRD SPINAL FIXATION SYSTEM, FIREBIRD SIDE-LOADING BODY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER FREE (YELLOW) VINYL PATIENT EXAMINATION

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 2, 2025

    ENDO STITCH

    FDA Adverse Event
    Injury ·DAVIS & GECK CARIBE LTD·Product code OCW·August 19, 2025

    UNKNOWN #3 PCA STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·July 13, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 14, 2013

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008

    MAGNETOM Skyra fit. Model Number: 10849580.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025

    UNKNOWN ENDO STITCH INSTRUMENT

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code GDW·June 2, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023