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Sources: EU EUDAMED, US FDA
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Dolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOLPHIN is a single-use, sterile inflation device used in cardiovascular procedures to pressurize (inflate) and depressurize (deflate) balloon catheters. The device itself consists of two components - the inflation device and large volume syringe (30 cc). The manually operation of the DOLPHIN is achieved by the manipulation of a large handle to drive a piston housed within the body of the device. Careful and controlled inflation is achieved by rotating the handle clockwise. During inflation a unique cam locking mechanism maintains pressure even if the user lets go of the device. Instantaneous deflation, regardless of balloon size, is made possible by the release of the dual locks located on device as well as a large, 30 cc syringe that is sold with each Dolphin Inflation Device. All the while during inflation or deflation pressure is displayed and can be monitored on a large analog gauge mounted on top of the device.
FDA Recall
Terminated
·Vascular Solutions, Inc.·Product code MAV·April 12, 2017
Merit Inflation Syringe Kit. Catalog Number KOS-02857
FDA Recall
Terminated
·Merit Medical Systems, Inc.·Product code MAV·August 25, 2016
Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is designed to be used to inflate / deflate balloon catheters as well as to monitor pressure within the balloon. The Everest 20atm Device is outfitted with a manometer with measuring pressures ranging from vacuum to 20bars in 0.5 bar increments. The Everest 30atm Device is outfitted with a manometer with measuring pressures ranging from vacuum to 30bars in 0.5 bar increments. The manometers are accurate to within +/- 3% of the gauges full scale. The device is a sterile, single use device and is not implanted; it also does not come in direct contact with the patient. This product is packaged in an inner and outer Tyvek /poly layer pouch.
FDA Recall
Terminated
·Medtronic Vascular·Product code MAV·February 6, 2014
Viceroy Inflation Syringe, 60mL, without gauge.
FDA Recall
Terminated
·Merit Medical Systems, Inc·Product code MAV·October 21, 2005
IntelliSystem II Thermal Dot Matrix printer 110 V adapter and fiber optic serial interface 10m cable
FDA Recall
Terminated
·Merit Medical Systems, Inc·Product code MAV·November 7, 2005
IntelliSystem II Thermal Dot Matrix printer 220 V 50 Hz adapter and fiber optic serial interface 10m cable.
FDA Recall
Terminated
·Merit Medical Systems, Inc·Product code MAV·November 7, 2005
Medtronic Everest 30 Disposable Inflation Device, AC3200. Used to inflate/deflate balloon catheters as well as to monitor pressure within the balloon.
FDA Recall
Terminated
·Medtronic, Inc.·Product code MAV·July 16, 2010
Synthes Inflation System (03.804.4135) Product Usage: Inflation system is used during kyphoplasty or other interventional kyphoplasty or other interventional procedures, to create and monitor pressure In the balloon catheter and pressure In the balloon catheter and to to deflate the balloon catheter
FDA Recall
Terminated
·PEROUSE MEDICAL ROUTE DU MANOIR Ivry Le Temple France·Product code MAV·October 6, 2014
Medtronic Everest 20 Disposable Inflation Device, AC2200. Used to inflate/deflate balloon catheters as well as to monitor pressure within the balloon.
FDA Recall
Terminated
·Medtronic, Inc.·Product code MAV·July 16, 2010
PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices).
FDA Recall
Terminated
·Abbott Vascular·Product code MAV·July 3, 2018
DeRoyal(R) Dolphin Inflation Device, REF 0185ND, Rx Only, STERILE EO, Dolphin is an inflation device indicated during angioplasty procedures to inflate and deflate the balloon catheter, and control pressure.
FDA Recall
Terminated
·DeRoyal Industries Inc·Product code MAV·June 7, 2017
Perouse Flamingo, Model 0218TA and 0218TB intended for use during cardiovascular procedure to create, maintain and monitor pressure in the balloon catheter.
FDA Recall
Terminated
·Perouse Medical 135, Route Neuve Irigny France·Product code MAV·May 10, 2012
Medtronic Everest 30 Disposable Inflation Device, AC3205P. Used to inflate/deflate balloon catheters as well as to monitor pressure within the balloon.
FDA Recall
Terminated
·Medtronic, Inc.·Product code MAV·July 16, 2010
IntelliSystem II Thermal Dot Matrix printer 110 V adapter and fiber optic serial interface 10m cable
FDA Recall
Terminated
·Merit Medical Systems, Inc·Product code MAV·November 7, 2005
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND
FDA Recall
Terminated
·PEROUSE MEDICAL ROUTE DU MANOIR Ivry Le Temple France·Product code MAV·April 5, 2017
Viceroy Inflation Syringe, 60mL, Sterile, Rx only.
FDA Recall
Terminated
·Merit Medical Systems, Inc·Product code MAV·October 21, 2005
IntelliSystem II Thermal Dot Matrix printer 220 V 50 Hz adapter and fiber optic serial interface 10m cable.
FDA Recall
Terminated
·Merit Medical Systems, Inc·Product code MAV·November 7, 2005
Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended for use during cardiovascular to create and maintain, monitor pressure in the balloon catheter - balloon inflation device for angioplasty procedures
FDA Recall
Terminated
·PEROUSE MEDICAL ROUTE DU MANOIR Ivry Le Temple France·Product code MAV·October 6, 2014
Encore(TM) 26 Inflation Device, REF Catalog Nos.: (a) H74904526011, (b) M001151050, (c) M00566670, (d) M0067101140
FDA Recall
Terminated
·Boston Scientific Corporation·Product code MAV·June 15, 2017
MAYO MN XCOATED 3/8X1/2 AV 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