35 results · 16ms · Sources: EU EUDAMED, US FDA

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Membrane Changer Single-Use, REF MC, each package contains 3 changers; Membrane Changer Reloadable, REF MC-R, each package contains 3 changers; and Membrane Changer Insert, REF MC-I, each package contains 5 inserts. All are components of the Sentec Digital Monitoring System (SDMS).

FDA Enforcement
Class II ·Ongoing·SenTec AG·September 27, 2023

Medtronic Micra MC1VR01, Single chamber transcatheter pacing system, REF MC1VR01US (US only). Cardiac pacemaker.

FDA Enforcement
Class II ·Terminated·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·September 18, 2019

VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM) 4-0 UND VICRYL SUTURE 18"(45CM) 2-0 VIO VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM) 2-0 VIO VICRYL CT VIO 8X18IN 0 S/A CT-1 CR VICRYL SUTURE 18"(45CM) 1 VIO VCL CT UD 8X18IN 2-0 S/A CP-2 CR VCL CT VIO 8X18IN 3-0 S/A SH-1 CR VICRYL CT VIO 8X18IN 2-0 S/A SH CR VICRYL CT UD 8X18IN 2-0 S/A CT-1 CR VICRYL CT UD 8X18IN 0 S/A CT-1 CR VCL CT UD 8X18IN 1 S/A CT-1 CR 9 VICRYL SUTURE 18"(45CM) 0 UND VICRYL CT VIO 8X27IN 0 S/A CT-1 CR VICRYL SUTURE 27"(70CM) 1 UND VICRYL CT UD 8X27IN 0 S/A CT-1 CR VICRYL SUTURE 27"(70CM) 0 VIO

FDA Enforcement
Class II ·Terminated·Ethicon, Inc.·April 24, 2019

NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: 48135, 48135E

FDA Enforcement
Class II ·Ongoing·Mc3 Inc·March 27, 2024

NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: (1) 48145; (2) 48145E

FDA Enforcement
Class II ·Ongoing·Mc3 Inc·March 27, 2024

Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model 3025975. Product Usage: Water Purification System is intended to be used as a dialysis accessory to produce water through reverse osmosis for use with hemodialysis equipment..

FDA Enforcement
Class II ·Terminated·Mar Cor Purification·March 26, 2014

Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Usage: The device is intended to be used in surgery on fingers or toes to provide a blood-less field.

FDA Enforcement
Class II ·Terminated·Mar-Med Co·February 10, 2021

Mar Cor Purification CWP Reverse Osmosis System. Models 101, 102, 104, and 106.

FDA Enforcement
Class II ·Terminated·Mar Cor Purification·March 19, 2014

Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse osmosis system with the intended use of producing water for dialysis of multiple patients.

FDA Enforcement
Class II ·Terminated·Mar Cor Purification·May 14, 2014

Spacelabs ARKON Anesthesia Workstation. Spacelabs ARKON Anesthesia Workstation 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.

FDA Enforcement
Class II ·Terminated·Del Mar Reynolds Medical, Ltd.·July 31, 2013

BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are anesthesia gas machine. In most cases, the customer ordered both a BleaseFocus anesthesia workstation and a 700/900 ventilator. In some cases, the customer may order a 700/900 stand-alone ventilator would could be used with a BleaseFocus anesthesia workstation at a later date.

FDA Enforcement
Class II ·Terminated·Del Mar Reynolds Medical, Ltd.·December 26, 2012

Arkon Anesthesia Delivery System, Model 99999. Product Usage: Continuous Ventilator The Arkon Anesthesia Delivery System is designed to provide emergency oxygen, vaporized agent delivery and manual ventilation in the event of a power failure scenario. Clinicians are able to use Emergency O2 and manually ventilate the patient, providing gas and agent. However, the anesthesiologist will not have access to mechanical ventilation or ventilator monitoring.

FDA Enforcement
Class II ·Terminated·Del Mar Reynolds Medical, Ltd.·March 22, 2017

Spacelabs Healthcare Arkon Anesthesia Delivery System is intended for use in the hospital environment and operating room. Absorber Adapter Assembly Service Kit, part number: 050-9045-00. Absorber Adapter Assembly, part number: 650-1648-01. Arkon Absorber Canister Carrier, part number: 380-0916-01.

FDA Enforcement
Class II ·Terminated·Del Mar Reynolds Medical, Ltd.·May 24, 2017

Spacelabs Pediatric Flow Sensor Kit, PN: 376-0561-00. This kit is for Spacelabs Healthcare Blease 700/900 Series Ventilators. Designed specifically for the mechanical ventilation of adult and pediatric patients under general anesthesia.

FDA Enforcement
Class II ·Terminated·Del Mar Reynolds Medical, Ltd.·April 29, 2015

Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: 5955460 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Enforcement
Class II ·Terminated·Davol, Inc., Subs. C. R. Bard, Inc.·June 11, 2014

Composix" LP with Echo PS" 10x13 HUXH0294 HUXL0314 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Enforcement
Class II ·Terminated·Davol, Inc., Subs. C. R. Bard, Inc.·June 11, 2014

Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Enforcement
Class II ·Terminated·Davol, Inc., Subs. C. R. Bard, Inc.·June 11, 2014

Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: 5955800 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Enforcement
Class II ·Terminated·Davol, Inc., Subs. C. R. Bard, Inc.·June 11, 2014

Bard¿Ventralight" ST Mesh with Echo PS" 10"x13" Reorder Number: 5955113 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Enforcement
Class II ·Terminated·Davol, Inc., Subs. C. R. Bard, Inc.·June 11, 2014

Bard¿ Composix" LIP Mesh with Echo PS" 7"x9" Reorder Number: 0144790 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

FDA Enforcement
Class II ·Terminated·Davol, Inc., Subs. C. R. Bard, Inc.·June 11, 2014