14 results · 19ms · Sources: EU EUDAMED, US FDA

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ATRICURE DISSECTOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

POSITRACE DUAL MODE PET/CT ONCOLOGY SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

MICROPAQ, MODELS 402, 404

FDA 510(k)
FDA Class 2 ·Cardiovascular

LINEAR 7.5 FR. 25CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019

LINEAR 7.5 FR. 25CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019

COVER, BURR HOLE

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code GXR·July 1, 2016

ACL ADVANCE

FDA Adverse Event
INSTRUMENTATION LABORATORY CO.·Product code JPA·July 13, 2005

MATRIXMANDIBLE SHORT CUT PLATE CUTTER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HTZ·April 8, 2013

PULSAR MAX SR

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008

VENTAK PRIZM 2

FDA Adverse Event
Malfunction ·GUIDANT CLONMEL IRELAND·Product code LWS·April 6, 2011

LINEAR 7.5 FR. 40CC IAB

FDA Adverse Event
Injury ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·May 14, 2020

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. The following models are not available in the US: models N106, N107, P106, P107. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. Indicated for patients who are at risk for sudden cardiac death due to ventricular arrhythmias and may require pacing support.

FDA Enforcement
Class II ·Terminated·Boston Scientific CRM Corp·October 23, 2013

Brand Name: ¿ cobas c 6000 MODULAR Series System e 601 ¿ cobas c 8000 MODULAR Series System - e 602 ¿ Roche / Hitachi MODULAR Analytics Combination System Model/Catalog/Part Number: MODULAR Analytics E 170 ¿ 03022109001 ¿ 03023109973 ¿ 03739040001 ¿ 03739040692 ¿ 05023572001 ¿ 05023599001 cobas e 601 module ¿ 04745922001 ¿ 04745922692 ¿ 05036348001 ¿ 05036348692 ¿ 05860652001 cobas e 602 module ¿ 05990378001 The Roche/Hitachi MODULAR Analytics System (E170) is a fully automated, random-access, software- controlled system for immunoassay and photometric analysis intended for qualitative and quantitative in vitro determinations using a wide variety of tests. The cobas 6000 series (e 601) is a fully automated, random-access, software-controlled system for immunoassay and photometric analysis intended for qualitative and quantitative in vitro determinations using a wide variety of tests. It is optimized for high throughput workloads in the professional environment using a combination of Ion selective electrodes (ISE), a photometric analysis unit an immunoassay analysis module. The cobas 8000 Modular Analyze Series (e602) is a fully automated system for Clinical chemistry analysis, intended for the in vitro qualitative and quantitative determination of analytes in body fluids. It is optimized for high throughput workloads in the professional environment using a combination of ion selective electrodes (ISE) and a photometric analysis unit.

FDA Enforcement
Class II ·Terminated·Roche Diagnostics Corporation·January 24, 2018