BEUDAMED
    39 results · 23ms · 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 ×

    EM-4000 Specular Microscope

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Mini Port

    FDA UDI
    Covidien LP·20884521066295·Introducer

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293364·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049552·K-Wires, Double diamond threaded, .062-inch (1....

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771012955·K-Wires, Double diamond threaded, .062-inch (1....

    INTEGRAL X-SERIES HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304650428·

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100868·MCNEILL GLOBAL FIXATION RING LARGE

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071713133B0·Ring Curette Bayonet #3 lat angle custom

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071713131B0·Ring Curette Bayonet #3 custom

    TROJAN-ENZ BRAND

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BINAXNOW COVID-19 ANTIGEN SELF TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·February 2, 2022

    SELEX/MAGNUM MOD HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 24, 2018

    M2A-MAGNUM TPR INSRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 14, 2019

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 14, 2014

    VERSAMED IVENT

    FDA Adverse Event
    Injury ·VERSAMED MED. SYSTEMS·Product code CBK·July 15, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·September 22, 2008

    M2A-MAGNUM PF CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 14, 2019

    M2A-MAGNUM MOD HD

    FDA Adverse Event
    Injury ·.·Product code LPH·November 14, 2019

    COCR FEM HD 40MM TYPE 1 +9MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·November 12, 2019