BEUDAMED
    15 results · 24ms · Sources: EU EUDAMED, US FDA

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    Schoelly Cystoscopes/Hysteroscopes and Accessories

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

    Oticon

    FDA UDI
    Oticon A/S·05707131284945·H16V2, RITE 312 WL CBE

    ESI

    FDA UDI
    FTT MEDICAL, INC.·B3961501580·REPLACEMENT DILATING WINDOW FOR YEOMAN SIGMOID...

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100080·TEMPORAL SPECULUM OPEN WIRE

    Tibial Trial Tray Size 3

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215074081·

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 21, 2017

    ILLUMINATING SINUS SEEKER

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    SINCLAIR SEBORRHEA EMULSION

    FDA 510(k)
    FDA Unclassified ·Unknown

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 6, 2011

    GYNECARE GYNEMESH* PS

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTO·June 6, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 7, 2014

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    SHAFT FOR 90° SCREWDRIVER

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code DZI·March 3, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019