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

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    ECHO SOUNDER, ES-102EX

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

    Conmed/Linvatec

    FDA UDI
    Provision·B504OM50231430·

    Reprocessed Micro Sagittal Blade, Coarse, 9.5 x 25 x 0.6mm

    FDA UDI
    SURETEK MEDICAL·B39050231431·

    Conmed/Linvatec

    FDA UDI
    Provision·00810041065681·

    MedSource Waterproof Tape

    FDA UDI
    MEDSOURCE INTERNATIONAL LLC·00816703023464·Water Proof Tape, 1/2 x 5 Yd

    NA

    FDA UDI
    STERILMED, INC.·10888551019460·SAW BLADE MICRO SAGITTAL COARSE

    NA

    FDA UDI
    STERILMED, INC.·10888551017015·SAW BLADE MICRO SAGITTAL COARSE

    CONMED

    FDA UDI
    Conmed Corporation·10845854001929·MICRO SAGITTAL BLADE, COARSE, 9.5 X 25.5 X 0.4 MM

    BENZODIAZEPINES

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MILLENNIUM BLADES, MODEL MB101

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    OSSEOSPEED TX 3.5S - 13 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·July 19, 2023

    OSSEOSPEED TX 3.5S - 13 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·August 22, 2023

    BD LUER-LOK TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·September 9, 2019

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·March 3, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·March 3, 2026

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LGW·March 27, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·February 24, 2011

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 3, 2008

    COBAS 8000 ISE 900 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 13, 2023

    VUELOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020