24 results · 16ms · 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.

BPB medica CEMIX, PRODUCT NUMBER KVTMIXN, Vertebroplasty-Kyphoplasty cement mixing system

FDA Enforcement
Class II ·Terminated·BIOPSYBELL S.R.L.·May 26, 2021

BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP, 187 mm, 10G, RES RESWTR1112C-US

FDA Enforcement
Class II ·Terminated·BIOPSYBELL S.R.L.·May 26, 2021

BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT, 110 mm, 11 G, REF OBE1111

FDA Enforcement
Class II ·Terminated·BIOPSYBELL S.R.L.·May 26, 2021

Proton therapy system -Proteus 235 aka Proteus Plus. A medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·May 24, 2017

Maquet Getinge-BEQ-T 4906 PEDIARIC CPB PACK Material: 701056041

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular, LLC·June 5, 2019

Maquet Getinge-BEQ-TOP 30901 CUSTOM CPB PACK Material:701063071

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular, LLC·June 5, 2019

Maquet Getinge-BO-TOP 30901 CUSTOM CPB PACK Material: 701055372

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular, LLC·June 5, 2019

Medtronic Custom Perfusion Systems, indicated for use in the extracorporeal circuit during cardiopulmonary bypass (CPB) surgical procedures.

FDA Enforcement
Class II ·Terminated·Medtronic Perfusion Systems·February 14, 2018

CPB CATHETER KIT- DR.VAN TRIGHT. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·June 27, 2012

CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·June 27, 2012

CPB Catheter Kit Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior vena cava.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 30, 2014

CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypass procedures.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 4, 2012

CPB CATHETER KIT-DR BARTLES Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypass procedures.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 4, 2012

CPB CATHETER KIT-DR GERHARDT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypass procedures.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 4, 2012

CUSTOM CPB CATHETER KIT-DR. Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypass procedures.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 4, 2012

CPB CATHETER KIT- DR HENDRICKSO Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypass procedures.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 4, 2012

CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypass procedures.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 4, 2012

CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary bypass procedures.

FDA Enforcement
Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 4, 2012

Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during cardiopulmonary bypass (CPB) or similar procedures with extracorporeal circulation, which require continuous monitoring of the arterial and/or venous blood parameters: partial pressure of oxygen (pO2), temperature (TArt and TVen), oxygen saturation (SO2), hemoglobin (Hb) and hematocrit (Hct).

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular Us Sales, Llc·November 18, 2020

Single Basin Kits, Sterile-.Kits containing the Devon Light Glove Catalog Number/Description: 573509 7696-GSL-VL SINGLE BASIN KIT 573558 7665-CPB SINGLE BASIN KIT 573561 7696-KSC SINGLE BASIN KIT 31145645 7608 Single Basin KIT 31153060 7697-T4 Single Basin Kit 50000568 7605-SEC Single Basin Kit 50000599 7694-ADA Single Basin Kit 50007698 7698-T4 Single Basin Kit 50007699 7699-T4 Single Basin Kit

FDA Enforcement
Class II ·Terminated·Covidien LLC·July 29, 2015