BEUDAMED
    9 results · 33ms · 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.

    QUANTA LITE CMV IGG ELISA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Venture 038 catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDPOR ATTRACTOR IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SPIROPERFECT

    FDA Adverse Event
    Malfunction ·MEDIKRO OY·Product code BZG·August 11, 2023

    ENDOPATH DILATING TIP TROCAR

    FDA Adverse Event
    Malfunction ·EES-JUAREZ·Product code GCJ·February 19, 1997

    HARMONIC SCALPEL LAPAROSONIC COAGULATING SHEARS

    FDA Adverse Event
    Malfunction ·EES-SMITHFIELD·Product code KNS·February 19, 1997

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 27, 2011

    ENTERPRISE TSUNAGU SET CAP KIT

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDI·July 31, 2014

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·September 21, 2007