BEUDAMED
    27 results · 23ms · Sources: EU EUDAMED, US FDA

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    Calix Lumbar Spinal Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780130505·Integra® Jarit® Yankauer Suction Tube, Tip Only...

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306820601·Westcott Scissors slightly curved 22mm sharp ti...

    SUNMED GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRESSURE MANOMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·February 5, 2002

    Widex

    FDA UDI
    Widex A/S·05706069923902·WIDEX MOMENT MBB3D 30 (Silver grey)

    Widex

    FDA UDI
    Widex A/S·05706069787757·WIDEX EVOKE E-FM (Silver Grey ) 30, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069897722·WIDEX EVOKE E-FP (Silver Grey ) 30, Telecoil, V...

    Widex

    FDA UDI
    Widex A/S·05706069896091·WIDEX EVOKE E-FA (Silver Grey ) 30, Telecoil, V...

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·October 14, 2014

    CONTAK RENEWAL TR

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NKE·July 20, 2011

    ENDO GIA ROTICULATOR 45-2.0 SULU

    FDA Adverse Event
    Injury ·CO IDIEN, FORMERLY US SUR·Product code GAG·June 6, 2013

    Blue-Vis, CIBASOFT VISITINT, daily wear contact lens. Lot 1170119, Expiration 2007/10, BC 8.9, DIA 13.8, SPH -1.50, CIBA Vision, Corp, Duluth, GA 30097, Made in USA.

    FDA Recall
    Terminated ·Ciba Vision Corporation·Product code LPL·November 12, 2002

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 30, 2017

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·January 30, 2017

    SINGLE USE GUIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 25, 2017

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 29, 2025

    GMK-REVISION TIBIAL AUGMENTATION SIZE 2/10MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·June 23, 2023

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·February 13, 2017