BEUDAMED
    11 results · 25ms · 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.

    EXTERNAL FUNCTIONAL NEUROMUSCULAR STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    Duo Ti Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7402974514·Duo Ti, 45 x 14mm, 15°

    HI-LO TEMP(R) GENERAL PURPOSE TEMPERATURE PROBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STRUNG TELFA NON-ADHERENT SPONGE

    FDA 510(k)
    FDA Class 2 ·Neurology

    1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·November 2, 2012

    TALENT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·February 22, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    ENDOSUTURE SUTURE

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·January 31, 2011

    FEMORAL COMPONENT OPTION FOR CEMENTED USE ONLY SIZE E RIGHT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2022

    ARTICULAR SURFACE WITH HINGE POST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2022

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026