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AiR-OxygEN BLENdER (diSS and NiST Connections) CAUTiON 300 Held Drive Northampton, PA 18067 USA Model No. PM5200 Series SAVE THESE iNSTRUCTiONS Federal (USA) law restricts this device to sale by or on the order of a physician. www.precisionmedical.com PM5300 Series...
RECEiViNg / iNSPECTiON Remove the Precision medical, Inc. Air-Oxygen Blender from the packaging and inspect for damage. If there is any damage, DO NOT USE and contact your Provider. iNTENdEd USE Precision medical, Inc. Air-Oxygen Blender dispenses a continuous and precise blend of medical air and USP oxygen via outlet ports to infant, pediatric and adult patients.
SAFETy iNFORMATiON - WARNiNgS ANd CAUTiONS Indicates an imminently hazardous situation dANgER which, if not avoided, will result in death or serious injury. WARNiNg Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury. Indicates a potentially hazardous situation CAUTiON which, if not avoided, may result in minor or...
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• An Oxygen Analyzer/monitor must be used to verify oxygen concentration. • Accuracy of oxygen concentration will be affected if bleed is not activated at flow settings below 15 lpm for the High Flow Blender, and 3 lpm for the Low Flow Blender. •...
Supply Pressure: 30 - 75 psi (2.1 - 5.2 bar) Mixed gas Stability: Connection Types: Blender Air-Oxygen PM5200 High Flow 15 - 120 lpm With both supply pressures at 50 psi (3.4 bar) with NO BLEED 2 - 100 lpm With both supply pressures at 50 psi (3.4 bar)
SPECiFiCATiONS dimensions: (without fittings) Weight: Shipping Weight: Operating Temperature Range: Transport / Storage Requirements Temperature Range: Humidity: Accuracy:* Pressure drop: Low Flow: High Flow: The Air-Oxygen Blender has been degreased for Oxygen Service prior to delivery. The Air-Oxygen Blender reverse gas flow complies with clause 6 of ISO 11195. The Oxygen Analyzer should comply with ISO 7767 to meet CE requirement.
COMPONENT dESCRiPTiON ITEM Oxygen Concentration dial A dial used for selecting oxygen concentrations between 21%-100%. The FiO This dial does not rotate 360°. The dial starts at 21% and ends at 100%. Primary Outlet Port A male DISS oxygen fitting with check valve that delivers flow when engaged to any controlling device, such as a flowmeter.
COMPONENT dESCRiPTiON ITEM Air inlet Fitting A male DISS or NIST air fitting with one way valve that is used to connect an air supply hose Alarm An audible alarm that sounds due to an excessive pressure drop or deletion of either gas supply. Manifold Outlet (Optional) manifold with 3 primary outlets.
ALARM TEST 1. The Air-Oxygen Blender is installed and the flowmeter is turned on. Disconnect or turn off the air supply line to the Air-Oxygen Blender. 2. The Blender should alarm with a loud whistle noise. The whistle indicates the alarm is operating correctly. 3.
3. To activate the bleed, turn the knurled collar until the bleed pin is engaged. Then slide the collar back until it contacts the cover. 4. Confirm the concentration of air/oxygen with an Oxygen Analyzer/monitor. 5. Confirm the flow of air and/or oxygen mixture to the patient. 6.
• Every year conduct the Operational Verification Procedure (OVP). • Every 2 years the Air-Oxygen Blender should be serviced. PM5200 (P/N 505407) • Refer to the Air-Oxygen Blender Service manual (P/N 504827) for complete details regarding further maintenance and testing.
TROUBLESHOOTiNg If the Air-Oxygen Blender fails to function, consult the Troubleshooting Guide below. If problem cannot be solved by using Troubleshooting Guide refer to the Air-Oxygen Blender Service manual (P/N 504827) available on the Internet; www.precisionmedical.com or consult your Provider. Problem Oxygen concentration...
LiMiTEd WARRANTy LiMiTATiON OF LiABiLiTy Precision medical, Inc. warrants that the Blender, (the Product), will be free of defects in workmanship and/or material for the following period: Two (2) years from shipment Should any failure to conform to this warranty appear within the applicable period, Precision medical, Inc.
dECLARATiON OF CONFORMiTy manufacturer: Authorized European Representative: Emergo Europe Product: model(s): mDD Class: Classification criteria: As delivered, the object of the declaration described above is in conformity with the requirements of mDD 93/42/EEC Annex II.3 and the following documents: Document Title ISO 14971 medical Devices - Application of Risk management...
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