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Cortisol Saliva Luminescence Immunoassay The IBL International Cortisol Saliva Luminescence immunoassay is intended for the in-vitro diagnostic quantitative determination of Cortisol in human saliva and for use as an aid in the diagnosis and treatment of adrenal disorders. The device is not intended for point-of-care settings.

FDA Enforcement
Class II ·Terminated·Tecan US, Inc.·September 5, 2018

Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies Model Numbers: Sensis Vibe Hemo 11007641 Sensis Vibe Combo 11007642 Sensis 10764561 Postprocessing Workstation 6648161 SIS Server 6648153

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·March 10, 2021

Alinity ci -series System Control¿Module, Part Number 03R70 01 Product Usage: The Alinity ci series System Control Module has a scalable design to provide full integration of clinical chemistry and immunoassay analysis. The Alinity ci series System Control Module includes a clinical chemistry module and an immunoassay module, each performing all sample processing activities, and a system control module to provide a single user friendly interface. Each system can be customized by combining one or more sample processing modules, in multiple configurations, with a system control module to form a single workstation. The Alinity i Processing Module is a fully automated immunoassay analyzer allowing random and continuous access, as well as priority and automated retest processing using chemiluminescent microparticle immunoassay (CMIA) technology. CMIA technology is used to determine the presence of antigens, antibodies, and analytes in samples.

FDA Enforcement
Class II ·Terminated·Abbott Gmbh & Co. KG·September 4, 2019

Cold Storage Solution, 2L, labeled as Waters IGL Cold Storage Solution, Catalog No. CSS/2000/US; and, Belzer UW Cold Storage Solution, Catalog No. BUW_002. Intended for the hypothermic flushing and storage of specific organs in preparation for storage, transportation, and transplantation into a recipient.

FDA Enforcement
Class II ·Terminated·Preservation Solutions, Inc.·April 25, 2018

The Brilliance CT Big Bore is a whole-body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data from the same axial plane taken at different angles. Model Numbers 728244 and 728243.

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·September 24, 2014

Arkon Anesthesia Delivery System with Arkon Software Version 2.70, Display Unit Assembly 650-1769-00 installed, and Model #: 99999. This system includes a ventilator. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and nitrous oxide in a controlled manner to various patient breathing circuits with or without the use of mechanical ventilator, and may be used for the delivery of anesthetic vapor by use of a dismountable vaporizer. The device is intended for use only by a suitably qualified physician.

FDA Enforcement
Class I ·Terminated·Spacelabs Healthcare, Ltd.·August 22, 2018

Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C, Single use only, Rx Only

FDA Enforcement
Class I ·Terminated·WEST PHARMA. SERVICES IL, LTD·February 6, 2019

Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only

FDA Enforcement
Class I ·Terminated·WEST PHARMA. SERVICES IL, LTD·February 6, 2019

Vial2BAG DC 13mm, REF 6070111, Single use only, Rx Only

FDA Enforcement
Class I ·Terminated·WEST PHARMA. SERVICES IL, LTD·February 6, 2019