BEUDAMED
    28 results · 25ms · Sources: EU EUDAMED, US FDA

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    Cartesion Prime, PCD-1000A, V10.7

    FDA 510(k)
    FDA Class 2 ·Radiology

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113356·CLEAR CORNEA KNIFE 2.8MM (BX/5)

    24M - Tampa Electric Co.

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113363·CLEAR CORNEA KNIFE 3.0MM (BX/5)

    NOBELACTIVE TIULTRA NP 3.5X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

    NOBELACTIVE TIULTRA NP 3.5X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

    AERODR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Stat Profile Prime Plus Analyzer System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 19, 2019

    HYDRUS MICROSTENT

    FDA Adverse Event
    Injury ·IVANTIS INC·Product code OGO·March 5, 2024

    VAXCEL PERIPHERALLY INSERTED CENTRAL CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code LJS·October 13, 2008

    SIGN I. M NAIL

    FDA Adverse Event
    Injury ·SURGICAL IMPLANT GENERATION NETWORK (SIGN)·Product code HSB·August 5, 2011

    URETEX SUPPORT PP KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·June 21, 2013

    ARCTIC FRONT ADVANCE® CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·March 29, 2024

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVN·December 13, 2023

    ACRYSOF IQ PANOPTIX TRIFOCAL IOL

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LLC - HUNTINGTON·Product code MFK·July 30, 2024

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 9, 2022

    Y-90 THERASPHERE

    FDA Adverse Event
    Injury ·BIOCOMPATIBLES UK LIMITED·Product code NAW·September 27, 2023

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·March 5, 2024

    UNK - SCREWS: 7.3 MM CANNULATED

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·November 3, 2023