15 results · 9ms · 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.

Centricity PACS RA1000

FDA Enforcement
Class II ·Ongoing·GE Healthcare, LLC·June 15, 2022

Centricity Enterprise Web

FDA Enforcement
Class II ·Ongoing·GE Healthcare, LLC·June 15, 2022

Centricity Radiology RA600

FDA Enforcement
Class II ·Ongoing·GE Healthcare, LLC·June 15, 2022

Centricity Cardiology CA1000

FDA Enforcement
Class II ·Ongoing·GE Healthcare, LLC·June 15, 2022

Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·October 13, 2021

Centricity Universal Viewer Zero Footprint Client

FDA Enforcement
Class II ·Ongoing·GE Healthcare, LLC·June 15, 2022

Diana Automated Compounding System, Diana Onco 3xx, Item No. ASN303 The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.

FDA Enforcement
Class II ·Terminated·ICU Medical, Inc.·April 20, 2016

ELEOS COLLAR STEM, CEMENTED, FLUTED, 13MM X 120MM. Model Number: HC-13120-03M. Component of Limb Salvage System with BioGrip.

FDA Enforcement
Class II ·Ongoing·Onkos Surgical, Inc.·June 4, 2025

ELEOS COLLAR STEM, CEMENTED, FLUTED, 15MM X 120MM. Model Number: HC-15120-03M. Component of Limb Salvage System with BioGrip.

FDA Enforcement
Class II ·Ongoing·Onkos Surgical, Inc.·June 4, 2025

(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX; (3) GE Universal Viewer 8.0, Model 5865740-00x.

FDA Enforcement
Class II ·Ongoing·GE Healthcare, LLC·August 31, 2022

GE Centricity PACS-IW versions 3.6.0 through 3.7.3.9 SP1, SP2, SP3 and 3.7.3 SPa10, Model Numbers: a) 2052831-00x b) 2050578-0xx c) 2090228-002 d) 2052782-00x

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·June 19, 2019

MYLA server HP Proliant: DL380-G8 and ML350-G6 version 3.xx computer application software. MYLA V3 is a computer application ("Middleware") based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s).

FDA Enforcement
Class II ·Terminated·bioMerieux, Inc.·May 27, 2015

Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA)

FDA Enforcement
Class II ·Ongoing·Defibtech, LLC·December 4, 2024

GE Healthcare Centricity Cardiology CA1000 (CA1000), Model Numbers: 1) 2033901-001; 2) 2038437-001; 3) 2038437-009; 4) 2038437-014; 5) 2038437-015 ; 6) 2038437-0XX; 7) 2109571-007; 8) 2109571-010; 9) 2109571-011; 10) 2109571-012; 11) MANLEGACY111; 12) MANLEGACY112; 13) MANLEGACY47; 14) P00011TS.

FDA Enforcement
Class II ·Ongoing·GE Healthcare·April 9, 2025

GE Healthcare Centricity Radiology RA600 (RA600), Model Numbers: 1) 2022296-001; 2) 2033901-001; 3) 2038437-001; 4) 2038437-011; 5) 2038437-012; 6) 2038437-013; 7) 2038437-014; 8) 2038437-0XX; 9) 2098071-004; 10) 2109571-002; 11) 2109571-006; 12) 2109571-010; 13) 2109594-009; 14) 2109594-011; 15) K2090PS; 16) K2090PTED; 17) MANLEGACY114; 18) MANLEGACY64.

FDA Enforcement
Class II ·Ongoing·GE Healthcare·April 9, 2025