33 results · 6ms · Sources: EU EUDAMED, US FDA

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AIA-900 Automated Immunoassay Analyzer performs three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric immunoassay.

FDA Enforcement
Class II ·Terminated·Tosoh Bioscience Inc·December 19, 2018

EasyOne Pro Respiratory Analysis System Pulmonary Function Testing Device, Model 3000-1

FDA Enforcement
Class II ·Terminated·NDDd Medical Technologies, Inc.·December 11, 2019

Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery.

FDA Enforcement
Class II ·Terminated·NuVasive Inc·July 29, 2020

EasyOne Pro LAB VOS Respiratory Analysis System Pulmonary Function Testing Device, Model 3100-1

FDA Enforcement
Class II ·Terminated·NDDd Medical Technologies, Inc.·December 11, 2019

Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.

FDA Enforcement
Class II ·Terminated·Pride Mobility Products Corp·July 11, 2012

Access Hi-Low Exam Tables, Model 6501-XX

FDA Enforcement
Class II ·Terminated·Brewer Company, LLC·August 1, 2018

Atellica IM HER-2/neu (H2n) assay, 50 Test Kit, Catalog No. SMN 10995591, UDI Codes: (01)00630414599151(10)98034139(17)20210130 and (01)00630414599151(10)32478139(17)20210130 Atellica IM HER-2/neu (H2n) calibrator, 2 Pack, Catalog No. SMN 10995592, UDI Code (01)00630414599168(10)22695A49(17)20201211 ADVIA Centaur HER-2/neu (H2n) assay, 50 Test Kit, Catalog No. SMN 10308994, UDI codes : (01)00630414471235(10)43157138(17)20210130 (01)00630414471235(10)81653138(17)20210130 (01)00630414471235(10)99728138(17)20210130 (01)00630414471235(10)24043138(17)20210130 (01)00630414471235(10)32477138(17)20210130 Advia Centaur Systems HER-2/neu (H2n) calibrator, 2 Pack, Catalog No. SMN 10308993, UDI Codes: (01)00630414471228(10)64661A48(17)20201112 (01)00630414471228(10)81211A48(17)20201112 (01)00630414471228(10)91743A48(17)20201112 (01)00630414471228(10)22124A49(17)20201211 Product Usage: This product is intended to be used for in vitro diagnostic use in calibrating the ADVIA Centaur systems HER-2/neu assay.

FDA Enforcement
Class II ·Terminated·Siemens Healthcare Diagnostics, Inc·October 28, 2020

VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents

FDA Enforcement
Class II ·Terminated·Ortho-Clinical Diagnostics·July 10, 2013

HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)

FDA Enforcement
Class II ·Terminated·LIEBEL-FLARSHEIM COMPANY LLC·July 14, 2021

InSite HER-2 Detection Kit, an immunohistochemistry assay for in vitro diagnostic use.

FDA Enforcement
Class II ·Terminated·Biogenex Laboratories, Inc.·July 30, 2014

VITROS 5600 Integrated System (product code 6802413) Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS Chemistry Products MicroTip Reagents and VITROS Immunodiagnostic Products Reagents.

FDA Enforcement
Class II ·Terminated·Ortho-Clinical Diagnostics·July 10, 2013

Philips/Children's Medical Ventures Smart Monitor 2 Professional Series infant apnea monitor.

FDA Enforcement
Class II ·Terminated·Childrens Medical Ventures·June 25, 2014

VITROS 4600 Chemistry System (VITROS 5,1 FS System family member)(product code 6802445) Product Usage: For use in the in vitro quantitative measurement of a variety of analytes of clinical interest, using both VITROS Chemistry Products Slides (colorimetric endpoint, rate, ion-selective electrode, and immunorate methods) and VITROS Chemistry Products MicroTip liquid reagents (spectrophotometric and spectrophotometric immunoassay methods.)

FDA Enforcement
Class II ·Terminated·Ortho-Clinical Diagnostics·July 10, 2013

Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer

FDA Enforcement
Class II ·Terminated·Roche Diagnostics Operations, Inc.·February 11, 2015

1) VITROS 5,1 FS Chemistry System (product code 6801375) and 2) VITROS 5,1 FS Chemistry System Refurbished (product code 6801890) Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS Chemistry Products MicroTip Reagents and VITROS Immunodiagnostic Products Reagents.

FDA Enforcement
Class II ·Terminated·Ortho-Clinical Diagnostics·July 10, 2013

ORTHO¿ Assay Software (OAS) Server, Catalog # 6842840 Usage: The ORTHO¿ Summit System (OSS) is a modular, integrated system for use with licensed blood screening tests. Consisting of networked processors and instruments linked together via a local area network, assay-specific pipetting protocols and ORTHO Assay Software (OAS), OSS automates many of the processing functions and data management requirements associated with ELISA (enzyme-linked immunosorbent assay) microplate testing.

FDA Enforcement
Class II ·Terminated·Ortho-Clinical Diagnostics·July 10, 2013

Japan DISP SET, 263J, 205J, HAR - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma

FDA Enforcement
Class II ·Terminated·Haemonetics Corporation·February 5, 2020

Artis zeego systems, model number 10280959, with serial numbers 1000-1599 : Artis zeego is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures.

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·November 19, 2014

JAPAN DISP SET, 261J, 205J, HAR - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and washing procedure before pumping the red cell product to either a bag for gravity reinfusion into the patient or an extracorporeal circuit.

FDA Enforcement
Class II ·Terminated·Haemonetics Corporation·February 5, 2020

REPAIR KIT, REF ARA101, UDI 884908083637 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.

FDA Enforcement
Class II ·Terminated·Medical Components, Inc dba MedComp·March 28, 2018