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

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    Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction with the EXENT assays.

    FDA Recall
    Open, Classified ·The Binding Site Group, Ltd.·Product code OTA·April 16, 2026

    Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement pumps, part #AI5511, a component of model numbers 756000 and 757000.

    FDA Recall
    Open, Classified ·Ohio Medical Corporation·Product code BTA·November 16, 2021

    MINISCAV (tm) Vacuum Pump

    FDA Recall
    Open, Classified ·R A Medical Services Holmes House Skipton Road Keighley United Kingdom·Product code BTA·August 23, 2023

    3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370

    FDA Recall
    Open, Classified ·3M Company·Product code BSB·April 10, 2025

    Infinity Central Station. Model Number: MS26800 The Infinity CentralStation (ICS) is intended for centralized monitoring of adult, pediatric and neonatal patient data within the hospital or clinical environment. Centralized monitoring involves the display and management of data from networked patient monitors including the annunciation of visual and audible physiologic parameter alarms at a central monitoring workstation.

    FDA Recall
    Open, Classified ·Draeger Medical Systems, Inc.·Product code MHX·January 14, 2025

    Dimension Vista Total Bilirubin (TBIL) Flex Reagent Cartridge; Siemens Material Number (SMN): 10445146;

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code CIG·July 30, 2024

    Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN

    FDA Recall
    Open, Classified ·Getinge Usa Sales Inc·Product code FQO·October 14, 2022

    INFX-8000V. For radiographic and fluoroscopic studies and intervention.

    FDA Recall
    Open, Classified ·Canon Medical System, USA, INC.·Product code OWB·January 31, 2022

    Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System

    FDA Recall
    Open, Classified ·Paragon 28, Inc. 14445 Grasslands Dr Englewood CO 80112-7062·Product code MBI·July 13, 2022

    DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile

    FDA Recall
    Open, Classified ·Medshape, INC.·Product code HWC·November 17, 2021

    Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

    FDA Recall
    Open, Classified ·IPG Medical Corporation·Product code GEX·May 5, 2026

    MAVERICK Measurement Module Spectrometer PN 820-01367 (originally part of a kit PN 820-01519) Finished Goods PN 820-01496

    FDA Recall
    Open, Classified ·REPLIGEN CORPORATION·December 10, 2025

    My3D Personalized Solutions Humeral Cup, Model Number: C24-0223-0003. It is a component of a Custom Constrained Shoulder Arthroplasty Device

    FDA Recall
    Open, Classified ·Onkos Surgical, Inc.·Product code QHQ·May 20, 2025

    MOSAIQ Oncology Information System

    FDA Recall
    Open, Classified ·Elekta, Inc.·Product code IYE·January 15, 2025

    Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05, 13894-16, 17550-08, 12236-18, 11854-15, 8043-29, 12466-17, 15599-17, 14764-09, 13194-16, 17069-09

    FDA Recall
    Open, Classified ·Alcon Research LLC·Product code LRO·February 10, 2025

    LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·September 29, 2023

    LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·September 29, 2023

    LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·September 29, 2023

    LIFEPAK 15, REF: 99577-001960, Part Number: V15-7-000026

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·September 29, 2023

    LIFEPAK 15, REF: 99577-001955, Part Number V15-5-000584 and V15-7-000020

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·September 29, 2023