BEUDAMED
    21 results · 22ms · Sources: EU EUDAMED, US FDA

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    Z-6 Atrioseptostomy Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PPS PI

    FDA UDI
    PEROUSE MEDICAL·03661234011377·Pressure Injectable Safety Huber Needle

    Kompressor™ Compression Screw System

    FDA UDI
    Ascension Orthopedics, Inc.·10381780280149·MINI TRAILING DRIVER

    Kompressor Compression Screw System

    FDA UDI
    Smith & Nephew, Inc.·00885556869017·MINI COMPRESSION DRIVER

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112366·CHUCK HANDLE #3K 10CM LONG

    Votion

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730007483·Votion 018 MC UR 4/5 HK -7T 0A 0O (10PK)

    Votion®

    FDA UDI
    Ortho Organizers, Inc.·00190707113247·Votion .018 MC UR 4/5 HK -7T 0A 0O (10PK) VOTION

    IN-FAST BONE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GLADIATOR HIP STEM

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·December 26, 2024

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·December 26, 2024

    INTELLIVUE INFO CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 19, 2023

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·February 14, 2025

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·May 1, 2024

    VAN PS OPEN INTL FEM-LT 70 70

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 16, 2021

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code HDD·October 20, 2008

    TRANSSEPTAL NEEDLE, BRK SERIES, ADULT 18 GA, 71CM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·August 10, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITI·July 8, 2013

    COMPREHENSIVE REVERSE CENTRAL SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 20, 2018

    COMPREHENSIVE STANDARD TAPER ADAPTOR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·March 20, 2018