12 results
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12ms
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Sources: EU EUDAMED, US FDA
CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser software. LAP isocenter marking control software. Laser systems for patient alignment.
FDA Enforcement
Class II
·Terminated·LAP of America Laser Applications, LLC·June 11, 2014
AVNS ambIT System - PIB/PCA W 2.5in Cath, Product Code: 220509
FDA Enforcement
Class II
·Terminated·Avanos Medical, Inc.·June 14, 2023
AVNS ambIT System - PIB/PCA W 5in Cath, Product Code: 220507
FDA Enforcement
Class II
·Terminated·Avanos Medical, Inc.·June 14, 2023
P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182, Sterile R, Single Use Only
FDA Enforcement
Class II
·Terminated·Paragon 28, Inc.·December 18, 2019
FLOW-I Anesthesia System The system is intended for use in administrating anesthesia while controlling the entire ventilation for patients with no ability to breathe, as well as in supporting patients with a limited ability to breathe.
FDA Enforcement
Class I
·Terminated·Maquet Cardiovascular Us Sales, Llc·July 18, 2012
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
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
Beacon Tip Torcon NB Advantage Catheter Catheter, Intravascular, Diagnostic
FDA Enforcement
Class II
·Terminated·Cook Inc.·August 31, 2016
NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·May 21, 2014
Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·July 9, 2014
Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·July 9, 2014
Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·August 28, 2013