BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Monster Screw System

    FDA UDI
    Paragon 28, Inc.·00889795153357·2.3 x 230 mm, K-wire, Single Trocar Tip, THREAD...

    cobas pulse blood glucose monitoring system

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    VERSATREK MYCO PZA KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 25, 2012

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 23, 2014

    INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·September 1, 2023

    SCREW-IN

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    OPTIFLOW

    FDA Adverse Event
    Death ·FISCHER AND PAYKEL HEALTHCARE LIMITED·Product code BZD·December 22, 2010

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KDI·July 23, 2014

    REDUCTION FORCEPS WITH SERRATED JAW-RATCHET 144MM

    FDA Adverse Event
    Malfunction ·SYNTHES TUTTLINGEN·Product code HTD·December 1, 2015