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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    VITALOGRAPH MODEL 7100 - VITALOJAK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902738715·INSTRUMENT 8110525 BENDING IRON

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756814270·RIGID COLLAR

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776172008·Lahey Gall Duct Forceps, right angle, long serr...

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K1102250·Tray, Base, 2.25", Universal

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K1104250·Tray, Base, 4.25", Arcamed

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K1104250·Tray, 4.25 Inch Base

    ARTHREX TENODESIS SCREW 7MM, 8MM, 9MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELITECH CLINICAL SYSTEMS GLUCOSE PAP SL ELITECH CLINICAL SYSTEMS ELICAL 2, ELITECH CLINICAL SYSTEMS ELITROL 1 AND 2

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ECHI GREENVILLE NC 2

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·November 22, 2011

    ECHI GREENVILLE NC 2

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·November 30, 2011

    BERKETTE BEACH CHAIR LIMB POSITIONER

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUCTS, INC.·Product code CCX·April 24, 2026

    STONYBROOK HSP NY NY 1

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code OEZ·September 15, 2015

    SERVO-S

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·April 5, 2013

    GEMSTAR 7 SP NEW

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·September 16, 2014

    UNICEL® DXC 600I ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 1, 2011

    C21785 IT TREVISO

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code GEI·December 14, 2012

    D731 MICRO 27 ARTERIAL FILTER WITH 27 MICRON PHISIO COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTM·May 18, 2022

    D731 MICRO 27 ARTERIAL FILTER WITH 27 MICRON PHISIO COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTM·March 17, 2022

    OVERTUBE

    FDA Adverse Event
    Malfunction ·FUJIFILM OPTICS INC., LTD.·Product code FED·January 20, 2012