BEUDAMED
    10 results · 25ms · 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 ×

    EMIT 2000 DIGOXIN ASSAY/CALIBRATORS MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MILLENNIUM

    FDA UDI
    Avalign Technologies, Inc.·00190776292362·Doane Knee Retractor

    FOUNDATION HYBRID COMPOSITE

    FDA 510(k)
    FDA Class 2 ·Dental

    STERILE SUTURE BOOTS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    B1005, ACUCISE ENDOPYELOTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code EYB·April 17, 2017

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 27, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·December 8, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 30, 2013

    UNKNOWN TEXTURED SALINE BREAST PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·September 21, 2023

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·October 25, 2024