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

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    HYDROXYLAPATITE

    FDA 510(k)
    FDA Class 2 ·Dental

    BoneCam

    FDA UDI
    MEDLINE INDUSTRIES, INC.·00818614020778·

    NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    E-Temp

    FDA 510(k)
    FDA Class 2 ·Dental

    SYRINGE S2 10ML 22GA 1-1/4IN BD CHINA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 12, 2019

    Widex

    FDA UDI
    Widex A/S·05706069421323·Widex CLEAR440 C4-m BTE (Winter silver ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069421330·Widex CLEAR440 C4-m BTE (Titan grey ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069421361·Widex CLEAR440 C4-m BTE (Winter silver/Black ) ...

    Widex

    FDA UDI
    Widex A/S·05706069421309·Widex CLEAR440 C4-m BTE (Warm beige ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069421354·Widex CLEAR440 C4-m BTE (Tan silk ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069421347·Widex CLEAR440 C4-m BTE (Midnight black ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069421316·Widex CLEAR440 C4-m BTE (Cappuccino brown ) RC ...

    BD SYRINGE S2 10ML 22GA 1-1/4IN BD CHINA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 12, 2019

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·April 17, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA INC.·Product code DTE·October 31, 2012

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·August 12, 2010

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·October 19, 2023

    Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781270. 2. Model Number (REF): 782113.

    FDA Enforcement
    Class II ·Ongoing·Philips North America·May 6, 2026

    Pinnacle Cups, Part numbers 121701048 121701050 121701052 121701054 121701056 121701058 121701060 121701062 121711048 121711052 121712050 121712052 121712056 121722048 121722050 121722052 121722054 121722056 121722058 121722060 121722062 121731048 121731050 121731052 121731054 121731056 121731058 121731060 121731062 121732048 121732050 121732052 121732054 121732056 121732058 121732060 121732062 121732064 - Product Usage: The PINNACLE CUP devices are part of the Pinnacle Hip Solution for the anatomic reconstruction of the hip joint, which promotes prosthetic joint load and function.

    FDA Enforcement
    Class II ·Terminated·DePuy Orthopaedics, Inc.·January 13, 2021