BEUDAMED
    2,674 results · 69ms · 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.

    SURFACE MEDICAL, INC.

    FDA registration
    SURFACE MEDICAL, INC.·5 products·🇨🇦 Canada

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 11, 2026

    INTRODUCER KIT FOR GASTROSTOMY FEEDING TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KGC·June 20, 2023

    Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA, 24 ENCA ASL 2104 Medium 8 x 15 Inch 1/EA, 24 ENCA ASL 2105 Large 8.5 x 17.5 Inch 1/EA, 24 ENCA ASL 2106 Extra-Large 9 x 20 Inch 1/EA, 24 ENCA ASL 2150 Universal 7 x 18 Inch 1/EA, 24 ENCA Medical - An arm sling is a device intended for medical purposes to immobilize the arm, by means of a fabric band suspended from around the neck.

    FDA Enforcement
    Class II ·Terminated·Owens & Minor Distribution, Inc.·December 28, 2016

    UNKNOWN CORTRAK NASOGASTRIC TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·December 31, 2025

    CORFLO NG/NI FEED TUBE WITH STYLET, ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·April 11, 2026

    CORFLO NG/NI FEEDING TUBE WITH STYLET, ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·February 6, 2026

    CORFLO NG/NI FEED TUBE WITH STYLET WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·April 16, 2026

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·November 12, 2020

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·December 13, 2016

    CORFLO NASOGASTRIC/NASOINTESTINAL PEDIATRIC FEEDING TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 20, 2026

    INTROCAN SAFETY

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code DQR·April 21, 2016

    CARTIVA

    FDA Adverse Event
    Malfunction ·CARTIVA·Product code PNW·February 25, 2022

    EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix Biopharmaceuticals Ltd. MDA blood bank, Sheba Hospital, Ramat-Gan, POB 888, Kiryat Ono 55000 Israel U.S. License No. 1603. Distributed by: Ethicon, Inc. P.O. Box 151, Somerville, NJ 08876-0151 USA. The Pressure Regulator System is positioned on the floor or on an IV pole and accepts medical gas (compressed air, nitrogen, CO2) from the central hospital system or from medical gas cylinders.

    FDA Enforcement
    Class II ·Terminated·Ethicon, Inc.·October 31, 2012

    IV KIT 100 CS

    FDA Adverse Event
    Injury ·MEDICAL ACTION INDUSTRIES·Product code LRS·January 6, 2026

    VICKS

    FDA Adverse Event
    Injury ·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·October 28, 2016

    VICKS

    FDA Adverse Event
    Injury ·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·June 16, 2017

    CARTIVA

    FDA Adverse Event
    Malfunction ·CARTIVA·Product code LXH·February 25, 2022

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·April 23, 2026

    ASTROGLIDE

    FDA Adverse Event
    Malfunction ·COMBE INC·Product code KMJ·January 16, 2024