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

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    Medussa-PL Cage

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777655·LUMBAMED BASIC DORSAL STAYS M SILVER III

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777600·LUMBAMED BASIC DORSAL STAY WM SILVER III

    Navigator 3 Wired Probe, 14 mm Angled

    FDA UDI
    crystal-photonics GmbH·04260152884484·gamma probe system, angled wired probe

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112687·BARRON CORNEAL PUNCH 9.25MM

    ACRA-CUT

    FDA UDI
    ACRA-CUT INC·00810607002839·Disposable Cranial Perforator

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780024842·Integra® Jarit® Volkman Retractor, 8-1/2", 6 Pr...

    BACK-UP MEIER STEERABLE GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERSATUBE TAPERED TRACHEOSTOMY TUBE WITH DISPOSABLE INNER CANNULA, MULTIPLE, PREFIXES C-VT, C-VTIC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Disposable Cranial Perforator

    FDA UDI
    ACRA-CUT INC·00810607000095·Cranial Perforator

    KIT DRAIN 100CC W/7MM PERF

    FDA Adverse Event
    Malfunction ·PR006 PUERTO RICO-ANASCO·Product code GCY·May 16, 2023

    Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Custom Anasthesia Breathing Systems; Multipac Anasthesia Breathing Systems - Product Usage: intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece.

    FDA Enforcement
    Class II ·Terminated·Intersurgical Inc·January 6, 2021

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    IPL QUANTUM

    FDA Adverse Event
    Other ·LUMENIS, LTD·Product code GEX·October 2, 2008

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·July 1, 2013

    BBL - MUELLER HINTON AGAR WITH 5% SHEEP BLOOD

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·October 18, 2022

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·September 15, 2022

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL.·Product code DTZ·March 12, 2024

    INSPIRE 7F

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·June 24, 2025

    INSPIRE 7F

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·February 5, 2025