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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    IMPRAFLO 3500 SERIES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NP UCLA Abutment Gold, Non-Hexed

    FDA UDI
    STERNGOLD DENTAL LLC·00841549111761·The UCLA-Type Abutment is attached directly to ...

    Rampart One Lumbar Interbody Fusion Device

    FDA UDI
    SPINEOLOGY INC.·M7404904515·Rampart One Screw

    ACUSON S228 TRANSDUCER FOR TRANSCRANIAL COLOR DOPP

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CUP: MPACT 3D METAL ACETABULAR SHELL Ø50 TWO-HOLE

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·April 5, 2022

    PD CYCLER 110 VOLT HOMECHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·November 22, 2010

    AUTOGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 1, 2014

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 4, 2012