BEUDAMED
    8 results · 22ms · 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 ×

    WONTECH Surgical Optic Fibers (BA400/BA400R/BA600/BA600R)

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

    SYNCHRON SYSTEMS PHOSPHORUS (PHS) REAGENT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    YARLAP

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

    CERTAIN¿ EP¿ HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 4MM(H)

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·December 9, 2022

    30 G X 1/2 IN. BD PRECISIONGLIDE¿ SPECIALTY USE STERILE HYPODERMIC NEEDLE

    FDA Adverse Event
    Injury ·BD MEDICAL (BD EAST) PHARMACEUTICAL SYSTEMS·Product code FMI·October 18, 2016

    ACCU-CHEK ACTIVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 19, 2008

    SABER X-L STRAIGHT GUARDED ATT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·September 2, 2011

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 22, 2013