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

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Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the vascular system over an appropriately sized wire guide.

FDA Enforcement
Class I ·Terminated·Cook Inc.·August 12, 2015

Slip-Cath Beacon Tip Catheter Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques.

FDA Enforcement
Class II ·Terminated·Cook Inc.·August 31, 2016

Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.

FDA Enforcement
Class II ·Terminated·Cook Inc.·November 27, 2019

Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the vascular system over an appropriately sized wire guide.

FDA Enforcement
Class I ·Terminated·Cook Inc.·August 12, 2015

Beacon Tip Torcon NB Advantage Catheter Catheter, Intravascular, Diagnostic

FDA Enforcement
Class II ·Terminated·Cook Inc.·August 31, 2016

Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.

FDA Enforcement
Class II ·Terminated·Cook Inc.·November 27, 2019

Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.

FDA Enforcement
Class II ·Terminated·Cook Inc.·November 27, 2019

White Lumax Guiding Coaxial Catheter Catheter, Percutaneous Intended for the delivery of angioplasty balloons and other types of interventional devices.

FDA Enforcement
Class II ·Terminated·Cook Inc.·August 31, 2016

Shuttle Select Slip-Cath Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques

FDA Enforcement
Class II ·Terminated·Cook Inc.·August 31, 2016

Evolve Cell Culture Bags, part numbers: EV1000N and EV3000N The Evolve bag is made of Ethyl Vinyl Olefin (EVO) and contains no BPA or latex. The bag can be supplied with tubing sets that can include, but are not limited to, the following components: EVA/PVC coextruded tubing, PVC tubing, Yconnectors, needle-free valves, female luers, male luers and/or caps

FDA Enforcement
Class III ·Terminated·OriGen Biomedical, Inc.·April 21, 2021

Dicken Eye Pack, part number CPA-3202-2. Product packaged in a convenient manner for use in a general clinical procedure

FDA Enforcement
Class II ·Terminated·Windstone Medical Packaging, Inc.·April 19, 2017

MEGA¿ 7.5Fr. 30cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK¿ MEGA¿ 7.5Fr. 40cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK¿ MEGA¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK¿ MEGA¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit, STATLOCK¿ & APA

FDA Enforcement
Class II ·Terminated·Datascope Corporation·June 15, 2016

REF 4890 SMARTSCRAPER CE0123, STERILE EO. Used in oral surgery.

FDA Enforcement
Class II ·Terminated·Meta C.G.M. Spa·June 9, 2021

REF: 3598 SAFESCRAPER TWIST, CE 0123, STERILE EO. Used in oral surgery.

FDA Enforcement
Class II ·Terminated·Meta C.G.M. Spa·June 9, 2021

Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·November 4, 2015

MULTIGENT Creatinine (Enzymatic), Catalog Numbers 8L24-31 and 8L24-41; IVD. Intended for the quantitative determination of creatinine in human serum, plasma, and urine using the ARCHITECT c Systems The product is a medical device (chemistry reagent) and is intended for the quantitative determination of creatinine in human serum, plasma, and urine using the ARCHITECT c Systems. The kit is provided as a ready to use liquid material consisting in two components: Reagent 1 and Reagent 2. According to the catalogue number, the kit is composed of three vials of 48 ml for Reagent 1 and three vials of 18 ml for Reagent 2 in the configuration 8L24-31. The configuration 8L24-41 consists in ten vials of 90 ml for Reagent 1 and ten vials of 34 ml for Reagent 2

FDA Enforcement
Class II ·Terminated·Sentinel CH SPA·August 9, 2017

Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·October 2, 2019

MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 8L25-30

FDA Enforcement
Class II ·Terminated·Sentinel CH SpA·October 2, 2019

Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of the Alinity c CRP Vario assay, Cardiac CRP high sensitivity method [Cardiac CRP], on the Alinity c analyzer.

FDA Enforcement
Class III ·Terminated·Sentinel CH SpA·October 13, 2021

REF 3987, SAFESCRAPER CURVE TWIST, CE 0123, STERILE EO. Used in oral surgery.

FDA Enforcement
Class II ·Terminated·Meta C.G.M. Spa·June 9, 2021