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

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    U&U Enteral Syringe

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517730800·CoRoent XL+, 8x18x55mm 15°

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517291967·CoRoent® XLFW, 8x22x55mm

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821608550·CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

    INTELLISPACE ECG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 28, 2024

    PREVENA PLUS INCISION MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC·Product code OMP·September 24, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    EXTRACTOR PRO RX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code FGE·July 13, 2011

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NIK·October 10, 2014