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

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    Filters Regulation: Us FDA ×

    SHARPS DISPOSABLE CONTAINERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471129450·K-WIRE - DOUBLE TROCAR WITH GUIDE 1.6mm DIA x 1...

    COPRA TEMP PMMA-DISK

    FDA 510(k)
    FDA Class 2 ·Dental

    ELEMENTS OBTURATION UNIT

    FDA 510(k)
    FDA Class 1 ·Dental

    DRILL F.RADIOLUCENT TARGETING DEVICE SIDEWINDER Ø3,2 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·September 16, 2013

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 23, 2014

    FOUNDATION KNEE

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code JWH·January 24, 2013

    COMBISET WITH BVM

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FJK·November 22, 2010