BEUDAMED
    12 results · 20ms · 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 ×

    BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BD ProbeTec™ ET CT/GC Amplified DNA Assay Collection Kit

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902201434·Swab Wet Male Urethral

    NEXT Medium Chocolate Mint Prophy Paste Box 200

    FDA UDI
    Preventech·D024220143·NEXT Medium Chocolate Mint Prophy Paste Box of ...

    FINGER RING RETRACTOR HOOK

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896077157·FINGER RING RETRACTOR HOOK SHARP TIPS

    ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VASOVIEW 5 HARVESTING CANNULA

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FUSA F8 (HF/PS/1.8/M)

    FDA Adverse Event
    Injury ·FUSA·Product code KDI·August 26, 1996

    IMPLANT, ENDOSSEOUS, ROOT-FORM

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·August 28, 2025

    RESOLUTION CLIP DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MND·October 31, 2008

    AC POWER MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·August 11, 2011

    FORTIFY ASSURA DR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025