BEUDAMED
    7 results · 27ms · 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.
    Filters Regulation: Us FDA ×

    PERMA-DOC PHANTOM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODEL 9444 TELETRACE II ECG MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ST AIA-PACK CYSTATIN C, MODEL 025217

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 6, 2025

    ARGONMEDICAL PICC CATHETER

    FDA Adverse Event
    ARGON MEDICAL·Product code LJS·February 6, 2013

    OT SELECT METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·February 16, 2011

    PROTECTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014