BEUDAMED
    8 results · 23ms · 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 ×

    Randox RX Daytona Plus Alkaline Phosphatase (ALP)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122285·KWire .062x9" (1.6x225mm)

    THERMEDX 37-5 ELECTROCAUTERY PROBES, MODELS MPJ200, MPJ210, MPS220, MPN230, BPH240

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    RINSPIRATION CATHETER SYSTEM, MODELS 50135, 550135, P7065, P70135

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD SYRINGE 10ML SALINE POSIFLUSH SAFESCRUB

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code QTI·January 2, 2026

    SM104 M-SERIES W/5TH WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 11, 2013

    SIEMENS ONCOR

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code IYE·July 8, 2011

    OLYMPUS

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FHN·September 5, 2008