BEUDAMED
    27 results · 24ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Radiology

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023318·600 Micron SU Thulio Performance 3m Fiber

    Classic by RISKONTROL

    FDA UDI
    ACTEON MANUFACTURING·03760243000508·Disposable single use tips for air/water syringe

    6450 RV2 MASK

    FDA UDI
    HANS RUDOLPH, INC.·00874750004881·DISP V2 LG FACE PC/HG/MASK ADP

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001546·CODMAN SLIM-LINE Aneurysm Clip 30 Degrees Forwa...

    Zodiac

    FDA UDI
    ALPHATEC SPINE, INC.·00844856063204·TI ILIAC BONE SCREW ASSY, 7.5MM X 65MM X 15°

    Zodiac

    FDA UDI
    ALPHATEC SPINE, INC.·00844856063211·TI ILIAC BONE SCREW ASSY, 7.5MM X 65MM X 30°

    ELITE MEDICAL INSTRUMENTATION

    FDA UDI
    ELITE MEDICAL INSTRUMENTATION·G569EMI7292016650·Rochester-Pean hemostatic artery forceps, curve...

    VERASENSE for Stryker Triathlon

    FDA 510(k)
    FDA Class 2 ·Neurology

    In-Ka Percutaneous Balloon Dilatation Catheters, Amplatz Sheath

    FDA 510(k)
    FDA Unclassified ·Unknown

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    Raw Surgical Corporation

    FDA UDI
    RAW SURGICAL CORPORATION·G508RSC7292016650·Rochester-Pean hemostatic artery forceps, curve...

    GE OEC 2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 21, 2008

    CAPSURE Z

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    ISOLINE

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA, S.R.L.·Product code MRM·June 28, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 20, 2012

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·April 2, 2019

    SMARTSET GHV GENTAMICIN 40G

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code MBB·May 8, 2025

    TC3 RP TIBIAL INSERT S5,20.0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·December 19, 2024

    LCS CRUC M/B PAT REPLC GVF LG+

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·December 19, 2024