BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PIV SYSTEM

    FDA 510(k)

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074088518·INSTRUMENT 2981032 10X32MM DSTRCTR TRIAL

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981032·anteriors; shade A2; mould BL2

    TR-USB TELEPHONIC STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Halcyon

    FDA 510(k)
    FDA Class 2 ·Radiology

    11MM/130 DEG TI CANN TFNA 440MM/LEFT - STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HSB·November 20, 2017

    PANORAMA SERVER

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·January 29, 2013

    HALO360 ABLATION CATHETER

    FDA Adverse Event
    Injury ·BARRX MEDICAL, INCORPORATED·Product code GEI·February 2, 2011

    L-CLIP APPL/REMVR 90 MM RND HANDLE VAR

    FDA Adverse Event
    Malfunction ·PETER LAZIC GMBH·Product code HCI·December 18, 2013

    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026