BEUDAMED
    18 results · 45ms · Sources: EU EUDAMED, US FDA

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    ONWARD Medical Inc.

    FDA registration
    ONWARD Medical Inc.·1 product·🇺🇸 United States

    ARC-EX

    FDA Adverse Event
    Injury ·ONWARD MEDICAL INC.·Product code SDO·March 25, 2026

    HOL ML 5MM ENDO APPLIER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDO·March 30, 2022

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·August 27, 2024

    HOL ML 5MM ENDO APPLIER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDO·March 30, 2022

    RENASYS GO NEGATIVE PRESSURE WOUND THERAPY

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW WOUND MANAGEMENT·Product code BTA·April 24, 2014

    ETHICON SECURESTRAP 5MM ABSORBABLE STRAP FIXATION DEVICE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GDW·December 1, 2021

    MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·May 10, 2023

    INFUSOMAT ®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·December 12, 2023

    PM050-N HYHSURGPN,7.5",EXP KT,-,OQ,5

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BSO·July 21, 2022

    CARELINK PERSONAL MMT-7333

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code CGA·January 22, 2023

    CARELINK PERSONAL MMT-7333

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code CGA·January 18, 2023

    CARELINK PERSONAL MMT-7333

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code CGA·January 16, 2023

    RENASYS GO NEGATIVE PRESSURE WOUND THERAPY

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW WOUND MANAGEMENT·Product code BTA·April 24, 2014

    GUARDIAN LINK 3 OUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·October 14, 2022

    INTROCAN SAFETY® 3

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·January 22, 2025

    Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21 Vial Labels: Mat. No K589911-21512

    FDA Recall
    Open, Classified ·Agilent Technologies, Inc.·Product code PPM·May 20, 2022

    Whatman Body Fluid Collection Paper 903, Ref: 10534790, for IVD use. Whatman Inc., Florham Park, NJ. The device is used by healthcare professionals in the collection and in-vitro storage of neonate blood.

    FDA Recall
    Terminated ·Whatman, Inc.·Product code JKA·May 19, 2009