BEUDAMED
    7 results · 17ms · 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.

    LKB 2164 MACRO-SPIN R CENTRIFUGE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NMI PICC III CATHETER, NMI HPICC III CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    XPECT GIARDIA LATERAL FLOW ASSAY, MODEL 2450020

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PRODISC CERVICAL IMPLANT

    FDA Adverse Event
    Injury ·Product code MJO·November 14, 2012

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·March 6, 2014

    INTERLINK(TM)CONTINU-FLO SOLNSET 3INJ SITES 10DPM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FPA·September 13, 2010

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026