BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    EXMOOR TEFLON LOOP REPLACEMENT PROSTHESIS

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517403247·CoRoent® XL, 10x18x45mm 10°

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981045·anteriors; shade A2; mould IM4

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756025423·SELF CLOSURE ELASTIC BANDAGE

    Gibralt Spine System

    FDA UDI
    Choice Spine, LP·00840996169912·GIBRALT,TAP,4.5

    DESTINATION RENAL GUIDING SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    A-33 DENTAL ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·February 19, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 24, 2014

    SULLIVAN VPAPII - AUSTRALIA.

    FDA Adverse Event
    Injury ·RESMED LTD.·Product code BZD·February 3, 2011