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

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    Guidion

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00195377109750·NTS Tubes Tray, Standard

    PROFYLE

    FDA UDI
    Stryker GmbH·04546540258212·Depth Measuring Gauge

    Ti-Fix OLIF Spacer

    FDA UDI
    Tyber Medical, LLC·M695P32101100·Ti-Fix OLIF Spacer 32 x 10 x 11 (mm) x 0 °

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C31422101100·Titanium PLIF Spacer, 22 x 10 x 11mm, 0 deg

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C30422101100·PEEK PLIF Spacer, 22 x 10 x 11mm, 0 deg

    InterPulse

    FDA UDI
    STRYKER CORPORATION·04546540683830·Handpiece Set with Bone Cleaning Tip and Suctio...

    InterPulse

    FDA UDI
    STRYKER CORPORATION·04546540861641·Handpiece Set with Coaxial Bone Cleaning Tip an...

    ATRIUM CENTRILFX MESH

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

    POWDER-FREE NITRILE EXAMINATION GLOVES, WHITE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ZENIX

    FDA UDI
    Zoll Medical Corporation·00198843000056·ZENIX, EMS STANDARD CONFIGURATION

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 26, 2025

    GMK-HINGE FIXED TIBIAL INSERT SIZE 5/17MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·October 18, 2023

    GMK HINGE AND REVISION TINBN COATED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 7, 2025

    GMK HINGE AND REVISION TINBN COATED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 18, 2025

    GMK-HINGE FIXED TIBIAL INSERT SIZE 4/12MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·March 22, 2024

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 17, 2008

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·August 3, 2011

    FLEXTEND II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 8, 2013

    GMK-REVISION TINBN COATED FEMUR REVISION PS SIZE 4 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 21, 2023