Nationwide Foreign: Austria, Australia, Bahrain, Bulgaria, Canada, Czech Republic, Denmark, Germany, Hungary, Italy, Jordan, France, Greece, Japan, Hong Kong, India, Italy, Norway, Poland, Portugal, Saudi Arabia, Spain, Sweden, Switzerland, UK.
Description du dispositif
CATH. GUIDE 8F SR3.0 W/SH LAUN Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. || Product Code: LA8SR30SH
Model Catalog: 960-344 (Lot serial: All Lots); Model Catalog: 9734240 (Lot serial: All Lots); Model Catalog: 960-347 (Lot serial: All Lots); Model Catalog: 9733184 (Lot serial: All Lots); Model Catalog: 9733183 (Lot serial: All Lots); Model Catalog: 9733182 (Lot serial: All Lots); Model Catalog: 9730946 (Lot serial: All Lots); Model Catalog: 9730945 (Lot serial: All Lots); Model Catalog: 9730944 (Lot serial: All Lots); Model Catalog: 9734304 (Lot serial: All Lots); Model Catalog: 9734299 (Lot serial: All Lots); Model Catalog: 9734301 (Lot serial: All Lots); Model Catalog: 9734303 (Lot serial: All Lots); Model Catalog: 9734298 (Lot serial: All Lots); Model Catalog: 9734300 (Lot serial: All Lots); Model Catalog: 9734302 (Lot serial: All Lots); Model Catalog: 9734238 (Lot serial: All Lots); Model Catalog: 9734239 (Lot serial: All Lots); Model Catalog: 960-345 (Lot serial: All Lots)
Worldwide, including USA, Canada, Romania, Chile, and Belgium
Description du dispositif
PADPRO ADULT Radiotranslucent Pad w/Medtronic¿ connector, REF/Catalog #2516M. RX ONLY. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes. Made in USA for: CONMED CORPORATION Utica, New York, 13502.
Worldwide Distribution: USA including states of PA, ND, MN, CA, AL, CO, MI, NY, AZ, and OH and countries of Sweden, Iceland, Latvia, Germany, Italy, Austria, Belgium, and France.
Description du dispositif
Medtronic Performer CPB-Universal R2100375. || Catologue Number R5100052. The Performer CPB System is an electromechanical extracorporeal support device used during cardiopulmonary bypass procedures. Manufactured by: RanD S.r.l 41036 Mendolla (MO) Italy. Distributed exclusively by Medtronic, Inc.
Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. The Paceart System can act as a Practice Management software application and is intended for use by facilities that provide services such as event monitoring, trans-telephonic pacemaker evaluation, and in-office evaluation of implanted cardiac devices.