Advanced Medical has long and effective experience in different areas of marketing and selling medical device business. It is committed to introduce every innovative breakthrough in medical to end users, and it has succeeded with it. We are very much interested in every advance in medical device, and we will be more than happy and committed to introduce a breakthrough to our market. We are covering Jordan / Middle East, and right now we are holding MIS, anesthesia, general surgery and cardiovascular surgery products.

Our business is our name. Emergency Medical Products, Inc. has been servicing the emergency medical supply, clinic, hospitals, law enforcement, safety, Industrial, and university needs of medical professionals for 36 years. Over 100,000 EMS, Fire/Rescue, Public Safety, doctors, nurses, and Healthcare agencies and professionals rely on EMP every day. We offer free ground shipping on most orders and 98 percent of all orders go out the same day!

Virobac II®

The Ulti-Mist® HME product line has the right product for any patient ranging from pediatrics to adults from intubated patients to patients with tracheotomies. These products offer superior humidification for both anesthesia and critical care applications. The Ulti-Mist HME and HME/Filters provide maximum protection for patients and staff members. The entire product line of Ulti-Mist HMEs and filters offer practitioners the highest quality product with economic efficiency in mind.

The Ulti-Mist® HME product line has the right product for any patient ranging from pediatrics to adults from intubated patients to patients with tracheotomies. These products offer superior humidification for both anesthesia and critical care applications. The Ulti-Mist HME and HME/Filters provide maximum protection for patients and staff members. The entire product line of Ulti-Mist HMEs and filters offer practitioners the highest quality product with economic efficiency in mind.

The Ulti-Mist product line has the right product for any patient, ranging from pediatrics to adult and from intubated patients to patients with tracheotomies. These products offer superior humidification for both anesthesia and critical care applications. The Ulti-Mist HME/Filter products provide maximum protection for patients and staff members. This entire product line of Ulti-Mist HMEs and filters offer practitioners the highest quality of humidification and filtration available today. It is the result of King System’s commitment to listen to our customers and design solutions that offer the highest quality product with economic efficiency in mind.

The Ulti-Mist product line has the right product for any patient, ranging from pediatrics to adult and from intubated patients to patients with tracheotomies. These products offer superior humidification for both anesthesia and critical care applications. The Ulti-Mist HME/Filter products provide maximum protection for patients and staff members. This entire product line of Ulti-Mist HMEs and filters offer practitioners the highest quality of humidification and filtration available today. It is the result of King System’s commitment to listen to our customers and design solutions that offer the highest quality product with economic efficiency in mind.

The Sandman Auto™ CPAP device was designed to be highly accurate, comfortable and intelligent in order to deliver optimal auto CPAP pressure. This premium CPAP device has pressure and flow sensing capabilities that detect apneas, hypopneas, inspiratory flow limitations and snoring so it can react with optimal pressure at all times, while only increasing pressure during obstructive events. The patients’ critical data is stored internally for easy analysis with the optional software, while the auto-calibration feature provides precise pressure delivery for nearly all mask and tubing combinations. INTUITIVE AND COMPACT Like all Sandman™ therapy devices, Sandman Auto is simple to operate and robust. It has backlit front-facing screen and buttons so that patients can make simple adjustments without needing to sit up and turn on the light. It is light-weight, has an integrated power supply, single power cord and unique integrated heated humidifier for more comfortable therapy. Features Compliance Capabilities • Recording of apneas and hypopneas with central/obstructive split • Recording of inspiratory flow limitations and snoring • Leak detection and reporting for each respiratory event • Approx. 200 sessions of 8 hours stored in embedded memory • Approx. 50 sessions of 8 hours available on memory card • Comprehensive Sandman™ therapy software

This advanced auto-CPAP model records up to 200 sessions of compliance data and includes other features of the 420S model. The auto-CPAP function automatically adapts to airway pressure needs.

The MedSystem III® infusion pump is designed for use with our dedicated. MedSystem III® pump administration sets. The MedSystem III® infusion pump dedicated sets provide a wide variety of needleless and standard IV sets, each featuring free-flow protection.

A state-of-the-art, pain management system that meets industry recognized standards for advanced error-reduction features in PCA pumps Product Features • Patient Safety • Optimize medication delivery safety features with CADD®-Solis medication safety software • Encourages safety and standardization for all pain management therapies • Individual Patient Care • IV PCA, subcutaneous, epidurals, nerve blocks, surgical site infusion therapies • Post-op, labor and delivery, trauma, pediatrics • Scalable Connectivity • Unique architecture provides flexibility to sustain your vision of future IT infrastructure needs • Supports best practices and enables continuous quality improvements

• Extremely Small and Lightweight • Transfer BP Data via the Internet • Networked, Internet ASP, and Stand-Alone (Single PC) Versions • HIPAA COMPLIANT! • Compares 2 Separate BP Profiles • Patient-Triggered Measurements • Day / Night Analysis • Averaged BP vs. Heart Rate • Stores up to 300 Readings • Uses Oscillometric Method • Tabular Reports and Graphs • No Electrodes or Microphone • Windows® PC-Based

Since joining the Quantel group in September 2007, WaveLight Aesthetic GmbH is responsible for the dermatological products within the group. The company distributes its products under the name Quantel Derma.

surgical instrument distributor

HCPro's Healthcare Marketplace is dedicated to bringing you the highest quality healthcare management resources available. Our products and services keep you informed of the latest regulations and standards, provide insightful examples and advice from industry experts, and offer practical and effective solutions so that you can do your job better.

Bacterial and Viral Filters

Bacterial and Viral Filters

Bacterial and Viral Filters

Bacterial and Viral Filters

The Secretion Solution High Moisture Return Maintains Sputum Consistency “Patient’s secretions from both groups [HWBH & ThermoFlo™ Filter] remained in the moderate or normal range. Total duration of mechanical ventilation ranged from 3 days to 30 days. In no case did we have any endotracheal tube occlusions.” 1 “Sputum consistency was similar using either HCH (ThermoFlo™) or HW

With circuitGuard™ at the proximal airway, bacteria and viruses have to travel through one filter into the circuit and then traverse back through a SECOND filter (on the next patient) in order for cross contamination to occur. 100 Compliance With the gas sampling port only on the circuitGuard™, and not o

O2 Humidified before delivery to patient  Inspiratory Gases are Optimally Humidified  High Moisture Output with Low Resistance to Flow

Features Proven patient comfort of C-Flex™ (REMstar Auto M Series with C-Flex) and A-Flex™ (REMstar Auto M Series with A-Flex) Digital Auto-Trak™ Sensitivity tracks and responds to each breath to trigger C-Flex Flow-based Smart CPAP system for use in the lab or home Proactive algorithm looks for and adjusts to the patient's need based on optimal and critical pressure levels Small and sleek design with true consumer appeal Unobtrusive tubing connection on back of unit 360 degree connection swivel for easy movement during sleep Primary, tactile control buttons for easy on/off, ramp and C-Flex setting change Primary buttons have backlight for easy activation, even in the dark Covered LCD display for advanced settings and reporting of therapy statistics and patient reminders Optional integrated heated or pass-over humidification platform Encore® Pro SmartCard® capability for enhanced compliance reporting of apnea/hypopnea index, elevated leak levels and snoring Enhanced compliance reporting statistics include humidification use and C-Flex setting Deluxe ramp capabilities allow a 0 - 45 minute time period with a patient-adjustable ramp start pressure Lightweight device weighs just o

Product Features Conveniently small size (weighs 1.54 pounds and measures 5.6" W x 2.9" H x 7.7" L). Wide pressure range (4 to 20 cm H20). Measures pressure at the mask, rather than the device, for a precise measurement and better comfort. Compatible with complete family of Puritan Bennett® CPAP interfaces, including the Breeze SleepGear™ CPAP Interface System. Ultra-quiet operation. Adjustable pressure calibration. Durable construction. Automatic voltage regulator. Altitude compensation feature. Optional D/C power supply. Automatic leak compensation. Adjustable ramp start pressure. Breathing compliance meter. Two-year warranty. Compatible with complete family of Puritan Bennett® CPAP interfaces, including the Breeze SleepGear™ CPAP Interface System. SilverLining® Data Management Software option.

Product Features Compact size (2.65 lbs. with heated humidifier and measures 6.9" W, 7.5" L, 4.7" H). Integrated heated humidifier for breathing comfort. Wide pressure range (3 to 20 cm H20). Ultra-quiet operation. Fluid-resistant, front-facing display screen. Automatic altitude and leak compensation. Memory card. Sandman™ therapy software. Automatic patient reminders. Large backlit buttons dim automatically. Single cord for CPAP and heated humidifier. Automatic internal universal switching power supply. Ability to run on an external battery. Respiratory events detection Auto calibration of entire patient circuit Advanced auto therapy options

The US Food and Drug Administration (FDA) has approved a novel artificial cervical disc, BRYAN, for the treatment of single-level cervical disc diseases like radiculopathy and/or myelopathy. The titanium-polyurethane disc, developed by Medtronic Inc, is implanted in milled pockets of adjacent vertebral bodies from C3-C7 to substitute a diseased or bulging natural cervical disc.

PEAK Surgical, Inc. has announced that the U.S. Food and Drug Administration (FDA) has granted the company 510(k) clearance to market its PEAK(R) Surgery System for cutting and coagulation of soft tissue during plastic and reconstructive, ENT (ear, nose and throat), gynecologic, orthopedic, arthroscopic, spinal and neurological surgical procedures. The company also announced that it has initiated a series of clinical studies, called the PRECISE Studies (Pulsed Plasma Radiofrequency Energy to ReduCe Thermal Injury and Improve Surgical HEaling), to evaluate the use of the PEAK Surgery System in plastic, gynecologic and oncologic surgery.

Covidien has announced the global launch of the RapidVac(TM) Smoke Evacuator System — a powerful, efficient device that quietly filters airborne contaminants from the operating room environment. The System, an advance in effective control of surgical smoke, features an ultra low penetration air (ULPA) filter with 99.9995 percent efficiency at trapping particulate matter as small as 0.12 microns. The device’s maximum air flow - how much air can be filtered through the system - is 30 percent greater than that offered by previous models, but it operates quietly, without contributing to the ambient noise in the O.R.

Starch Medical Inc. has announced the CE approval of its PerClot(TM) Polysaccharide Hemostatic System (PHS) and the StarFoam(TM) Absorbable Polysaccharide Hemostat. Introduction of PerClot(TM) PHS will commence this month in the European Union and other select international markets. The StarFoam(TM) Absorbable Polysaccharide Hemostat will launch during the 2nd quarter, 2009. PerClot(TM) PHS is an absorbable, surgical hemostat composed of Absorbable Modified Polymers (AMP(TM)). AMP(TM) technology incorporates sophisticated, plant-based polymer modification processes that yield biocompatible, polysaccharide particles. There is no thrombin, collagen, or other human or animal components in AMP(TM) particles.

Ophthalmologists at South Nassau Communities Hospital are using a new micro-incision ophthalmologic surgical system that allows ophthalmologists to perform cataract surgery through a single incision that is 2.2mm or smaller. Traditional, no-stitch cataract surgery requires an incision that is 33 percent larger. In addition to this latest innovation in micro-incision eye surgery, South Nassau ophthalmologists are among the first in the region to use a cataract surgery system that has three different surgical options. This allows them to develop surgical approaches that are tailored to the needs of each patient.

ATS Medical, Inc. has announced it has received U.S. Food and Drug Administration (FDA) approval for the ATS 3f(R) Aortic Bioprosthesis. This is the Company’s first entry into the $400-plus Million U.S. tissue valve market. Based on the precept that ‘Form Follows Function’, the ATS 3f Aortic Bioprosthesis is a revolutionary next generation stentless pericardial aortic tissue valve that is unlike any other replacement valve. The product is based on a proprietary valve design that reproduces the functional characteristics of the native aortic valve.

Researchers from the Stanford University School of Medicine have reported that fenoldopam mesylate, a selective dopamine 1 receptor agonist which is used intravenously for the treatment of hypertension in adults, can also be effective in producing deliberate hypotension in children scheduled to undergo a surgery. The study, according to the lead author, Dr. Gregory Hammer, affects pediatric labeling for fenoldopam and guides practitioners about appropriate intraoperative dosing for deliberate hypotension.

Dune Medical Devices, Ltd. has launched a crucial clinical trial of the MarginProbe™, the company’s intra-operative, real-time, positive margin detection system. The launch follows the investigational device exemption (IDE) approval from the U.S. Food and Drug Administration of its protocol during surgery for breast cancer. To determine how malignant the tumor margins are, the MarginProbe system uses Radio Frequency Spectroscopy to characterize breast tissue. A controlled trial concluded that application of the probe by surgeons during lumpectomy reduced the need for repeat surgeries by 56%.

Pioneer Surgical Technology, Inc. has announced that the human implantation of its nanOss(TM)- Cervical cage has been carried out successfully. Designed to work as a bone, the device was used for standard cervical fusion surgeries performed at hospitals in China. The biologic inter-body spacer was used in combination with routine rigid fixation. The nanOss technology makes it two times stronger than PEEK cages.

VertiFlex® Inc. has launched its Silverbolt™ Plus, a for posterior lumbar fixation solution. The system is designed to help surgeons in various types of approaches – open, mini-open and percutaneous, for fixation of the lumbar spine. The single instrument set, said Earl Fender, CEO, Vertiflex, will support a variety of surgical applications such as percutaneous dynamic stabilization and percutaneous delivery of vertebral levels. The company develops motion preservation technologies and minimally invasive solutions for the treatment of spine disorders.