BEUDAMED
    251 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 ×

    ICS IMPULSE

    FDA 510(k)
    FDA Class 2 ·Neurology

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169606449·SPACER 2122550 O25 23.5MM 12 DEG 16X50

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·54026704624435·RUSCH Color Coded Guedel Airway Length 50mm Tra...

    Bernafon

    FDA UDI
    Bernafon AG·05711584022832·IN3 ITCP, L BE INIZIA 3

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780377795·Integra® Jarit® Ferris-Smith Needle Forceps, 6-...

    SCOTT'S SELECT K-FILES 6/pk 25mm # 50

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77811225501·ENDODONTIC K-FILES (6/pack) Length: 25mm, Size:...

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180521472·RAMP EXIT GRAFT CARTRIDGE

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141301·ZEUS® LLIF 12mm x 25mm x 50mm x 14° TRIAL

    NA

    FDA UDI
    Summit Medical, Inc.·00385640002219·

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916134471·ZEUS®-L, Lateral Lumber Interbody Fusion Device...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916134426·Zeus-L, Lateral Lumber Interbody Fusion Device,...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141257·ZEUS® LLIF 12mm x 25mm x 50mm x 07° TRIAL

    COAMATIC LR ANTITHROMBIN, NOTE: LR=LIQUID REAGENTS

    FDA 510(k)
    FDA Class 2 ·Hematology

    CAPILLARYS HEMOGLOBIN, CAPILLARYS FLEX PIERCING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    ULTRASAFE X100L PNG CLEAR NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·February 5, 2021

    ULTRASAFE X100L PNG RASPBERRY NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·February 10, 2020

    S FLEX/FEP 1X24 T31/CS6 3/ODA

    FDA Adverse Event
    Injury ·COVIDIEN·Product code LDF·May 17, 2013

    MITEK ANTEROMEDIAL FEMORAL AIMER 7.5MM

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code LXH·September 26, 2014

    SPECTRAFLEX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 13, 2011

    ULTRASAFE X100L PNG RASPBERRY NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·January 26, 2021