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

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    ROTA-DAN RAPID ROTAVIRUS EIA KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Gelseal™ Cardiovascular Patch

    FDA UDI
    VASCUTEK LTD·05037881010458·Gelseal Gelatin Impregnated Knitted Cardiovascu...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150652·K-WIRE - SINGLE TROCAR THREADED 2.0mm DIA x 200mm

    Elite® Buccal Tubes Direct Bond

    FDA UDI
    Ortho Organizers, Inc.·00190707074746·Elite®.018 SAA U7L NL MINI OPTI-MIM -14T DB

    PREMISE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 22, 2014

    Tuned Self-Fitting Mobile App

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Powder Free Nitrile Examination Glove

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CC TIBIAL INSERT SZ 4, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 2, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013

    ACCU-CHEK ® PERFORMA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 6, 2011

    SELUTE PICOTIP

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·July 22, 2014

    CC TIBIAL INSERT SZ 3, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

    CC TIBIAL INSERT SZ 2, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 7, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 25, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 30, 2025

    CC TIBIAL INSERT SZ 2, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 13, 2023

    TRAPEZOID TIBIAL TRAY SZ 5F/5T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 25, 2024

    TRAPEZOID TIBIAL TRAY SZ 5F/5T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 30, 2025

    CC FEMORAL SZ 5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 27, 2025

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 9, 2024