BEUDAMED
    11 results · 19ms · 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.

    ERIKA HPF 100

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·April 25, 2023

    SPECTRA SP II, SPECTRA DENTA II

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

    Slow Wave DS8

    FDA 510(k)
    FDA Class 2 ·Dental

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·April 3, 2023

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·April 3, 2023

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·April 3, 2023

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 5, 2014

    ENPULSE

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·October 15, 2012

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWS·August 10, 2010

    PROPONENT DR SL (Model L201)

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