Instructions for Use
8 Pages
Preview
Page 1
Dialflow Regulator Instructions for Use
702-0084.14 October 2014
1.
Symbols Warning!
Indicates a potentially hazardous situation which, if not avoided, could result in personal injury to the user or others.
Caution!
Indicates a potentially hazardous situation which, if not avoided, could result in damage to the equipment or property. Attention, consult accompanying documents
Use no oil
0120
CE Marked to Medical Device Directive 93/42/EEC as amended by directive 2007/47/CE
No smoking
Service due date
1304X12345 YYMM
Date of manufacture identification
2.
Warnings and Cautions
2.1.
Warnings!
Read through this entire instruction manual before using or showing others how to use a Dialflow Regulator. As with all medical equipment, attempting to use this device without a thorough understanding of its operation may result in patient or user injury.
Medical oxygen is, or should be considered, a drug and may be used in critical treatments. Medical gases should only be used for medical purposes on the authority of a physician or authorised clinician and then strictly in accordance with their instructions.
Oxygen is not flammable however an oxygen enriched atmosphere will drastically increase the rate and severity of combustion. Oil and/or grease in the presence of an oxygen enriched atmosphere will become highly combustible. Oxygen must never be allowed to contact oil, grease or other hydrocarbon based substances. Do not use oil or grease on this Dialflow Regulator.
Never administer oxygen while smoking or when near an open flame.
Oxygen therapy may be a critical treatment. A regulated flowmeter should be used in strict accordance with the prescription and instructions of a physician. The effectiveness of supplemental oxygen therapy can only be determined by continuous monitoring of blood oxygen levels. It is essential that PaO2 or SpO2 monitoring is carried out when supplemental oxygen is prescribed.
The use of the BPR Medical oxygen regulators for gases other than compressed oxygen is expressly prohibited.
Never permit compressed medical gases to enter a regulator suddenly. Always open the cylinder valve slowly.
Never use medical gases from a cylinder without reducing the pressure through a suitable regulator intended for that gas.
Always close the cylinder valve when the regulator is not in use.
Never use oxygen as a pressure medium to purge obstructed pipelines or equipment, operate pneumatic tools or to build up any pressure in tanks.
Never install a pin index regulator Dialflow Regulator with more than one yoke seal between the valve and the regulator. Before attaching the regulator, verify that the post valve is not already fitted with a yoke seal.
Ensure that you have the correct regulator for the type of cylinder you are intending to use. Never attempt to fit a regulator to an incompatible cylinder.
Ensure that the threaded fittings or indexing pins on the regulator are properly mated and tightened before opening the cylinder valve.
Do not stand in front of a regulator outlet when opening the cylinder valve.
Before removing a regulator from a cylinder, fully close the cylinder valve and release all gas from the regulator.
Secure cylinders to a wall, stand or cart.
Do not use or store oxygen equipment near excessive heat (>50 °C or 125 °F) or open flame.
Only appropriately trained personnel working in controlled conditions must perform disassembly, assembly and testing of regulators and flowmeters.
Dialflow Regulators are not MRI compatible.
Flowmeters may be affected if the cylinder pressure is other than stated in the specifications.
The threaded bull nose cylinder connection for medical oxygen and medical air may be the same, ensure that you have the correct cylinder for the application. This regulator is only intended for use with oxygen.
The holes in the side of the body of the device are for venting gas in the event that the relief valve is activated. Do not obstruct these holes or interfere with the relief valve in any way.
These regulators are designed for use for cylinder pressures up to 20 000 kPa (3000 psi/200 bar). Do not attempt to connect BPR regulators to cylinders having fill pressures in excess of this value.
Do not submerge the device in any fluid. Ensure that no fluid is allowed to enter the inlet valve or the vent holes.
Ensure the device is not set between flow settings. If set between flow settings failure to provide therapy may occur. Display of flow value does not indicate flow is occurring.
2.2.
Cautions!
Device performance may be affected if it is stored or transported in temperature outside of the range -20 °C to +60 °C (-4 °F to +140 °F).
The Dialflow Regulator is not suitable for autoclaving.
3.
Functional Description Flow Selection Dial
Outlet Barb
Flow Indication Window
Vent
Cylinder Contents/ Pressure Gauge Cylinder Connection
3.1.
Intended Use The Dialflow Regulator is intended to deliver medical oxygen at one of eleven pre-set rates directly from a high pressure oxygen cylinder. Flow is indicated in litres per minute (l/min) and is visible through a window adjacent to the flow selection dial. Medical oxygen is or should be considered a drug and should only be used for medical purposes on the authority of a physician and then strictly in accordance with their instructions. Always refer to the medical oxygen product labelling.
3.2.
Technical Description The Dialflow Regulator reduces the high pressure of the oxygen cylinder to a safe, more manageable pressure for application to patients. There are many types of oxygen cylinder connection used and these may be different from one country to another, ensure that this regulator is the correct connector for the cylinder to be used. Once connected to an oxygen cylinder, and with the cylinder valve opened, the user may select the flow rate prescribed by rotating the gas flow selection dial until the correct flow rate is seen in the viewing window. The rate at which gas flows from the regulator is controlled by a hole of known size and accuracy. Each flow rate has a different size hole. The output connector allows the user to connect an oxygen facemask, cannula or other application device as appropriate.
4.
Operating Instructions
4.1.
Preparation and Connection Check that the cylinder type and regulator inlet connector are compatible. Check the presence and condition of the input connector seal, which for pin index regulators is a washer type seal (Bodoc) and for bullnose regulators and O-ring. Fit the regulator to the cylinder ensuring that it is properly mated and the connectors are done up hand tight.
Turn the gas flow selection dial fully clockwise and check that the indication in the flowmeter window is zero. Open the cylinder valve slowly with a suitable cylinder key. Check the regulator cylinder contents gauge to verify that there is sufficient gas available. Connect a sufficient length of oxygen tubing (not supplied) to the outlet barb.
4.2.
Test Prior to Use Turn the flow selection dial to its highest setting and check that gas flow can be felt at the patient end of the tubing. If no medical oxygen flow is refer to Section 7 Troubleshooting of this manual. Turn off the oxygen flow by turning the flow selection dial fully clockwise.
4.3.
Operation Connect the free end of the oxygen tubing to the patient or patient enclosure using the appropriate connector (not supplied). Determine the appropriate oxygen flow rate in litres per minute (l/min) require for the patient. Turn the flow selection dial until the required rate is visible in the flow indication window; the dial ‘clicks’ into place and is obvious to the touch. Continue to monitor the patient as advised by the clinician. Check the regulator contents gauge regularly.
4.4.
After Use Upon completion of the therapy, turn the flow selection dial to zero, close the cylinder valve and disconnect the outlet hose from the regulator and the patient. To remove the regulator from the cylinder, first ensure the cylinder valve is closed. Bleed off any residual gas pressure in the regulator by turning the flow selection dial to any flow setting until flow ceases. Remove the regulator from the cylinder.
5.
Maintenance
5.1.
Interim Inspection All Dialflow Regulators should be inspected and tested on an annual basis to ensure correct performance.
5.1.1.
Cleaning Wipe down the outside of the device with an alcohol wipe. Do not allow the ingress of water or other solution into the device. Check the exterior condition of the device. Pay particular attention to the input connector seals, which should be replaced if damaged or missing. Check that the holes in the side of the device, which are designed to vent gas in the event of relief valve activation, are not obstructed or have otherwise been tampered with.
5.1.2.
Internal Leak Test Connect the regulator to a cylinder in accordance with this Instructions for Use. Set the flow selection dial to zero and open the cylinder valve. Connect a hose to the outlet barb and immerse the other end of the hose into water. Check for leak through (internal leak). Remove the hose.
5.1.3.
External Leak Test Attach a fresh, dry hose to the outlet barb and connect the other end of the hose to a calibrated flowmeter in the correct range for the device under test.
5.1.4.
Flow Test Verify flow rates at all flow settings against those given in the Device Specification.
5.2.
Service It is recommended ranges A and E be serviced every 2 years, ranges C and D every 4 years to ensure the device continues to perform in accordance to its specification. All Dialflow Regulators have a Service Due date on their label, indicating when the next service is due. Warning! Servicing must be carried out by a suitably qualified person working in a controlled environment. Full details of the recommended servicing requirements can be found in the Service Manual. The Service Manual can be obtained from your local BPR Medical distributor, details of which can be found at www.bprmedical.com. Complete the service in accordance with the instructions given in the Service Manual or return the device to a recognised BPR Medical Service Centre on or before the date shown.
6.
Specification
Specification
Value
Flow Accuracy
±15 % of setting for flow rates above 1 L/min +20 % - 10 % of settings of 1 L/min and below
Input Pressure Range
900 to 20,000 kPa (9 bar to 200 bar) Range A: 0, 0.02, 0.03, 0.05, 0.08, 0.12, 0.2, 0.3, 0.5, 0.75, 1.0, 3.0
Flow Settings (l/min)
Range C: 0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.5 Range D: 0, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 5.0, 6.0, 8.0, 10.0, 15.0 Range E: 0, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 1.0
Varying Inlet Pressure:
Typically less than 15 % change across the input pressure: Minimum: 900 kPa Maximum: 20 000 kPa
Varying Outlet Pressure:
Less than 1 % of reading up to 5 kPa (50 cm H2O) back pressure
Effects on Accuracy
Typically 0.2 % of reading per degree Celsius Transport/Storage/Operation: -20 °C to +60 °C (-4 °F to +140 °F) Humidity: 0-100 % RH non-condensing CE: Medical Device Directive 93/42/EEC - Class llb FDA: Class 1 Health Canada: Class 2 - Licence No: 83602 Varying Temperature:
Environmental
Regulatory
Applied Standards AS 2473.3
AS 3840.1
BS EN ISO 10524-1
Valves for compressed gas cylinders Part 3: Outlet connections for medical gases (including pin-indexed yoke connections) Pressure regulators for use with medical gases Part 1: Pressure regulators and pressure regulators with flow-metering devices Pressure regulators for use with medical gases. Pressure regulators and pressure regulators with flow-metering devices
BS EN ISO 14971
Medical devices. Application of risk management to medical devices
BS EN ISO 15001
Anaesthetic and respiratory equipment. Compatibility with oxygen
BS EN ISO 15002
Flow-metering devices for connection to terminal units of medical gas pipeline systems
BS EN ISO 15223-1
Medical devices. Symbols to be used with medical devices labels, labelling and information to be supplied. General requirements
BS EN 13544-2+A1
Respiratory therapy equipment. Tubing and connectors
BS 5682
Specification for probes (quick connectors) for use with medical gas pipeline systems
7.
Troubleshooting
Fault
No gas flow
Internal/external leak Insufficient gas flow
8.
Possible Cause
Solution
Gas cylinder turned off
Check gas supply
Dial-Flow Regulator not connected properly
Check gas specific probe is correctly connected
Gas cylinder empty
Replace gas cylinder
Filter blocked
Service or repair is required
Flow selection dial set to ‘0’
Select a positive flow rate
Seal failure
Service or repair is required
Filter partially occluded
Service is required
Supply pressure too low and/or gas cylinder nearly empty
Check gas supply and/or replace gas cylinder
Parts and Spares List
Part Number
Description
818-0040
Dial-Flow Regulator - O2 Range A - Pin Index/Barb
818-0041
Dial-Flow Regulator - O2 Range C - Pin Index/Barb
818-0043
Dial-Flow Regulator - O2 Range E - Pin Index/Barb
818-0051
Dial-Flow Regulator - O2 Range D - Pin Index/Barb
Spare Parts and Servicing 212-0012
Pin Index Yoke Seal
212-0048
Bullnose seal (Benelux)
303-0030
Cylinder Gauge Boot
303-0060
Swivel Cylinder Gauge, 0.3mm Restriction
9.
Distributor Details
Australia BOC Healthcare Customer Service Centre 10 Julius Avenue North Ryde Sydney NSW, 2113 T: +61 (0)2 8874 4400 F: +61 (0)2 9886 9000 www.boc.com.au New Zealand BOC Healthcare Customer Service Centre 970-992 Great South Road Penrose 1061 Auckland T: +64 (0)9 525 5600 www.boc.co.nz
BPR Medical Limited
T: +44 (0)1623 628 281
22 Hamilton Way, Mansfield
F: +44 (0)1623 628 289
Nottinghamshire
NG18 5BU, United Kingdom
www.bprmedical.com