BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    MALLINCKRODT DAR HEATED WIRE BREATHING CIRCUIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993268·anteriors; shade B4; mould BL

    APrioCore Plus

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    INTELLIVUE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·March 7, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011

    REVEAL LINQ

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code DSI·August 8, 2014

    TRABECULAR METAL 56MM CUP SIZE REVISION SHELL

    FDA Adverse Event
    Injury ·ZIMMER TMT·Product code LPH·April 9, 2026

    TRABECULAR METAL ACETABULAR REVISION SYSTEM ACETABULAR AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER TMT·Product code LPH·December 31, 2024

    HGP II ACETABULAR BONE SCREW SELF-TAPPING 50 MM LENGTH 6.5 MM DIA

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·August 5, 2024

    HGP II ACETABULAR BONE SCREW SELF-TAPPING 40 MM LENGTH 6.5 MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·August 5, 2024

    BONE SCREW SELF-TAPPING 6.5 MM DIA. 50 MM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·August 5, 2024

    TRABECULAR METAL REVISION SHELL 56MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 1, 2024

    TRABECULAR METAL ACETABULAR REVISION SYSTEM ACETABULAR AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 15, 2025