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

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    MEDSCOPE 4MM ARTHROSCOPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867052130·DRILL GUIDE, 2.6/1.35MM

    QKO (TM) AMYLASE B-HA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MR 700 MICROPLATE READER 012-700-1000

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FAST-CATH¿ HEMOSTASIS INTRODUCER, CATH-LOCK¿ LOCKING HUB, 12 CM SHEATH, 8.5 F

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DYB·January 22, 2024

    CORE MICRO DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·November 4, 2010

    SYSTEM 83 PLUS

    FDA Adverse Event
    Malfunction ·CUSTOM ULTRASONICS INC·Product code KOG·February 19, 2014

    LIGASURE IMPACT THORACIC

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·November 16, 2012

    RATCHETING ADAPTER, CANNULATED

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code LXH·May 7, 2022

    RATCHETING ADAPTER, CANNULATED

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code LXH·May 9, 2022

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020