Pda Occlusion Device

NEW XIENCE SIERRA STENT DESIGN The new XIENCE Sierra Stent Design, with Slim Flex Technology, has a lower crossing profile1 and greater post-dilatation expansion NEW STENT DELIVERY SYSTEM FOR COMPLEX CASES Design innovations built to provide the flexibility, crossability, and pushability needed for even the most complex cases. The XIENCE V®, XIENCE nano®, XIENCE PRIME®, XIENCE PRIME® LL, XIENCE Xpedition®, XIENCE Xpedition® SV and XIENCE Xpedition® LL , XIENCE Alpine®, and XIENCE SierraTM (XIENCE Family) of Everolimus Eluting Coronary Stents on the MULTI-LINK VISION® or MULTI-LINK MINI VISION® Delivery System INDICATIONS The XIENCE Sierra stent system is indicated for improving coronary artery luminal diameter in patients, including those with diabetes mellitus, with symptomatic heart disease due to de novo native coronary artery lesions (length â?¤ 32 mm) with reference vessel diameters of â?¥ 2.25 mm to â?¤ 4.25 mm. In addition, the XIENCE Sierra stent system is indicated for treating de novo chronic total coronary occlusions. CONTRAINDICATIONS The XIENCE Sierra stent system is contraindicated for use in: Patients who cannot tolerate, including allergy or hypersensitivity to, procedural anticoagulation or the post-procedural antiplatelet regimen. Patients with hypersensitivity or contraindication to everolimus or structurally related compounds, or known hypersensitivity to stent components (cobalt, chromium, nickel, tungsten, acrylic, fluoropolymers), or with contrast sensitivity. WARNINGS It is not recommended to treat patients having a lesion that prevent complete inflation of an angioplasty balloon. Judicious patient selection is necessary because the use of this device carries the associated risk of stent thrombosis, vascular complications, and/or bleeding events. This product should not be used in patients who are not likely to comply with the recommended antiplatelet therapy.

Developed for the treatment of mitral valve stenosis, the V-Broaden PTMC Balloon Catheter is indicated for Percutaneous Transvenous Mitral Commissurotomy in patients with hemodynamically significant mitral valvular stenosis, resulting primarily from commissuralfusion of the mitral valve cusps. The V-broaden PTMC Balloon catheter is manufactured of polyvinyl chloride with a balloon attached to the distal end. The balloon is consisted of two latex layers, between which is polyester micromesh. Product Specification/Models Specifications: 30mm/28mm/26mm/24mm/22mm/20mm. ETO sterilized, for single use. - USE sterilization.

Developed for the treatment of mitral valve stenosis, the v-broaden ptmc balloon catheter is indicated for percutaneous transvenous mitral commissurotomy in patients with hemodynamically significant mitral valvular stenosis, resulting primarily from commissuralfusion of the mitral valve cusps. The v-broaden ptmc balloon catheter is manufactured of polyvinyl chloride with a balloon attached to the distal end. The balloon is consisted of two latex layers, between which is polyester micromesh. Product specification/models Specifications: 30mm/28mm/26mm/24mm/22mm/20mm. Eto sterilized, for single use. Shelf life is 2 years.

Supplier: Cardiac interventional device, PTMC balloon, ASD closure device, PDA closure device, VSD closure device

Double channel syringe pump Specifications Applicable syringe: Any standard syringe with 10mló20ml(30ml)and 50ml(60ml) Accuracy: 2% (after the correct calibration) Delivery rate range: 50ml(60ml)¦0.1ml/h½1800.0ml/h (0.1ml/h step) 20ml(30ml)¦0.1ml/h½800.0ml/h (0.1ml/h step) 10ml¦0.1ml/h½400.0ml/h (0.1ml/h step) Time mode range: Sol.Vol.¦0.1½999.9ml (0.1ml step) Time¦1½1999min (1min step) Body weight mode range: Sol.Vol.¦0.1½999.9ml(0.1ml step) Drug mass¦0.1½999.9mg(0.1mg step) Dose¦0.01½99.99ug/kg/min(0.01ug/kg/min step) Weight¦0.1½300kg(0.1kg the least step) Volume limit range: 0½1999.9ml (0.1 ml step) Total volume range: 0.1½1999.9ml (0.1 ml step) Purge rate: 50ml(60ml)¦1800.0ml/h, 20ml(30ml)¦800.0ml/h, 10ml¦400.0ml/h Kvo rate: 1ml/h Alarms: near empty, syringe empty, volume complete(a volume limit has been set), occlusion, syringe loose, operation error, low battery and other device failures. Power source: Ac power supply: ac 100 to 240v10%¼50/60hz+ Internal li battery: 11.5v, 2000mah. Battery life with continuous operation is approx. 8 hours(when using a new, full charged battery and running at 5ml/h with any standard of syringe). Power consumption: 25va Dimensions: 300mmß240mmß250mm Net weight: approx. 3.5kg

Intended Use: To aid voicing to take place without the need for finger occlusion. The Trachie-Voice low profile speaking valve fits securely to a 15mm connector tracheostomy tube. It has a one-way mechanism that opens when the patient breathes in, allowing air into the airway via the tracheostomy. The valve closes on expiration allowing air to follow the normal route of expiration through the mouth and nose, instead of the tracheostomy, permitting speech. Being hands free allows voicing to take place without the need for finger occlusion, so reducing possible infection and hygiene concerns. * For non-ventilated patients * Economical/low cost device * Lightweight reducing pressure on stoma site * Reduces hygiene and infection concerns * Ridged sides enabling quick application and removal * Supplied complete with storage box * Available on FP10 Prescription * Single patient use only * UK Manufactured * Latex-Free * CE Marked TSV/100 Trachie-voice Speaking Valve (White) Pack size 12 (6x2) TSV/150 Trachie-voice Speaking Valve (Blue) Pack size 12 (6x2)

Veterinary Medical Devices Veterinary Medical Equipment Manufacturers Veterinary Infusion Pump Features 1. History records 2. Four operation modes:Rate mode,drip mode,time mode,body weight mode. 3. Anti-reverse rotation detection 4. Various visual and audible alarms 5. Double CPU ensuring safe infusion 6. Real time display  7. 3 adjustable occlusion pressure settings Removable pump body,convenient for cleaning 8. 12 months warranty WONDCON Veterinary Infusion Pump Specifications Pumping Mechanism: Curvilinear peristaltic Occlusion Sensitivity: low, middle and high IV Set: Support a wide variety brands of infusion set including major manufacturers & selected local brands Air-in-line Detection: Ultrasound sensor detection with four levels of air in line alarm adjustable Flow Rate: 0.1~1200 ml/h � Power Supply, AC: 110/230 V (optional), 50-60 Hz, 25VA Purge, Bolus Purge when pump stops, bolus when pump starts.Bolus rate300 ~ 1200 ml/h,purge rate 600ml/h Battery: Rechargeable lithium polymer battery,7.4V,2100mAh operating time:about 6 hours at 25ml/h Charging time:10hs with power on, 3hs with power off.  Accuracy: Universal IV set: ±5% Battery Life: 3 hours at 25 ml/h VTBI: 0 ~ 9999 ml Working Condition: Temperature:5~40,relative humidity:10~95%, air pressure:86~106kPa Infusion Mode: rate mode, drip mode,time mode,body weight mode  Relative Humidity: 30-75% KVO Rate: 1 ~ 5 ml/h Atmospheric Pressure: 860-1060 hpa Alarms Visual and audible alarms: Door open, Air-In-Line, Occlusion,Infusion completion, infusion near over, Start reminder function, Low Battery, Battery depleted, malfunction etc. Additional Features: Real-time shift totals, automatic power switching,mute button, purge, bolus, history log, system memory Size&weight: 145100 120 mm(length width height) 1.4kg   Safety Classification: Class , type CF Volume Infused: 0-36000ml Water Proof Level: IPx3

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