BEUDAMED
    6 results · 21ms · 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 ×

    APLICARE ALCOHOL PREP PAD

    FDA 510(k)
    FDA Unclassified ·Unknown

    PRIZM KERATOME BLADE (B.D. MODEL), MODEL MK8530BD

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    HTFX-222

    FDA 510(k)
    FDA Class 2 ·Dental

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 27, 2014

    DERMABOND 2

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code MPN·November 15, 2012

    *

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL RUSCH·Product code BTR·August 20, 2010