25 results · 8ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

REF/Catalogue Number GSX0020A, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631018

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631032

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSXE0030B, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132620128 *Not distributed within the US

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSXE0030, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617661 *Not distributed within the US

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSX0025A, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631025 *Not distributed within the US

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSXE0025, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617647 *Not distributed within the US

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSXE0025B, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132620111 *Not distributed within the US

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSX0030H, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132648948 *Not distributed within the US

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617630 *Not distributed within the US

FDA Enforcement
Class II ·Ongoing·W L Gore & Associates, Inc.·November 3, 2021

CT Goldseal BrightSpeed 16 PWR TIO 2 YR

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·August 8, 2018

RKN130002, RHEO KNEE 2 YR WARRANTY, MD, CE, External lower limb prosthetic component

FDA Enforcement
Class II ·Ongoing·Ossur H / F·May 22, 2024

RKN130003, RHEO KNEE 3 YR WARRANTY, MD, CE, External lower limb prosthetic component

FDA Enforcement
Class II ·Ongoing·Ossur H / F·May 22, 2024

RKNXC0005, RHEO KNEE XC 5 YR WARRANTY, MD, CE, External lower limb prosthetic component

FDA Enforcement
Class II ·Ongoing·Ossur H / F·May 22, 2024

RKNXC0003, RHEO KNEE XC 3 YR WARRANTY, MD, CE, External lower limb prosthetic component

FDA Enforcement
Class II ·Ongoing·Ossur H / F·May 22, 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