Precision Medical 1MFA Oxygen Chrome Flowmeter Instruction Manual

FLOWMETER
Models: 1MFA, 4MFA, 6MFA
and 8MFA Series

Caution! U.S. Federal law restricts this device to sale by or on the order of a physician.

RECEIVING / INSPECTION

Remove the Precision Medical, Inc. Flowmeter from the packaging and inspect for damage. If there is any damage, DO NOT USE and contact your Provider.
INTENDED USE
The Flowmeter is intended for use by physicians, respiratory therapists and other authorized hospital personnel to administer selected doses of medical gases to a patient.
READ ALL INSTRUCTIONS BEFORE USING
This manual instructs a Professional to install and operate the Flowmeter.
This is provided for your safety and to prevent damage to the Flowmeter.
If you do not understand this manual, DO NOT USE the Flowmeter and contact your Provider.

SAFETY INFORMATION – WARNINGS AND CAUTION

WARNING
Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
CAUTION
Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury.
CAUTION
Used without the safety alert symbol indicates a potentially hazardous situation which, if not avoided, may result in property damage.
Operating Instructions
Symbol for “USE NO OIL”

WARNING

• Use Flowmeters only for their “Intended Use” as described in this manual.

• ALWAYS confirm prescribed flow before administering to patient and monitor flow on a frequent basis.

• Flowmeters may contain magnetic, ferrous material that may affect the results of an MRI.
  To Reduce the Risk of Fire or Explosion:

• ALWAYS follow ANSI and CGA standards for Medical Gas Products and Flowmeters and Oxygen Handling.

• DO NOT use or store oils, greases, organic lubricants or any combustible materials on or near this Flowmeter.

• DO NOT use near any type of flame or flammable/explosive substances, vapors or atmosphere.

• DO NOT smoke in an area where oxygen is being administered.

CAUTION

• Flowmeters must be operated with the Flow Tube in a vertical, upright position.
• Only personnel instructed and trained in its use should operate this Flowmeter.
• Ensure all connections are tight and leak free.
• Only use oxygen-safe leak detector.
• DO NOT autoclave.
• DO NOT gas sterilize with EtO (Ethylene Oxide).
• DO NOT clean with aromatic hydrocarbons.
• DO NOT immerse Flowmeter in any kind of liquid. This will void the warranty.
• The 1MFA3001, 4MFA1001 & 6MFA1001 Flowmeters may have a factory installed restrictor. Prior to use, check Flowmeter labeling for flow restrictions.
• The 1MFA3001, 4MFA1001 & 6MFA1001 Flowmeters contain a glass Flow Tube which is fragile. Special care should be observed to avoid breaking the Flow Tube.

SPECIFICATIONS

6-15 ±.50 l/min
0 — 26 1/min| 11/min| 2-4 ±.50 l/min 5-26 ±10% of reading
3- 35 Umin| 1 (3-15) Urn in 5 (15-35) l/min| 3-4 ± .50 1/min 5-35 ±10% of reading
0— 70 1/min| 5 l/min| 0-70 ±10% of reading

Flush Flow is the output of the flowmeter when the flow indicator is beyond the highest calibrated graduation. The Flush Flow range is as indicated on the flowmeter labeling.
Transport / Storage Requirements
-40˚F (-40˚C) to 140˚F (60˚C) The gas and inlet pressures are indicated on the Flow Tube or Flowmeter body.
NOTE: Storage / Transport outside the specified range may cause damage to the flowmeter.
The effect on accuracy of flow due to variations in ambient temperature is standard accuracy +7.3% @ 32°F (0°C) and -3.0% @ 104°F (40°C).
The above Flowmeter models are calibrated at specified inlet pressure, 70°F (21°C), standard atmospheric pressure. International models are calibrated per specifications marked on Flow Tube or Flowmeter body.
Specifications are subject to change without prior notice.
CAUTION

• DO NOT over tighten Knob when turning off. This will cause damage to the Flowmeter.
• Pressures other than those indicated on the Flow Tube or Flowmeter body may affect the accuracy of the indicated flow.
• Gas Temperatures other than 70° F (21°C) may affect the accuracy of the indicated flow.
• Attaching accessories to the outlet (which may increase resistance to outlet flow) may change indicated flow but will not affect the accuracy of the flow.
• ONLY use appropriate gas specific indexed fittings to connect Flowmeter to gas source. Use Oxygen connections for oxygen Flowmeters; use air connections for air Flowmeters.
• DO NOT attempt to repair the 8MFA Flowmeters. There are no serviceable parts.

CLEANING INSTRUCTIONS

1. Disconnect all connections before cleaning.
2. Clean exterior surfaces of the Flowmeter with a cloth dampened with a mild detergent and water.
3. Wipe dry with a clean cloth.

TROUBLESHOOTING

If the Flowmeter fails to function, consult your Provider or Precision Medical, Inc.

•Replace Body Assembly
Sticking Float Ball| •Debris in Flow Tube| •Clean Flow Tube & Float Ball
Unable to set desired flow| •Blocked Inlet| •Replace Body Assembly
Knob will not turn| •Valve seized| •Replace Body Assembly

8MFA Models DO NOT have serviceable parts.
RETURNS
Returned products require a Returned Goods Authorization (RGA) number.
Any product returned to Precision Medical, Inc. must be packaged in a sealed container to prevent damage. Precision Medical, Inc. will not be responsible for goods damaged in transit. Return Policy available at www.precisionmedical.com.

OPERATING INSTRUCTIONS

WARNING
Read this User Manual before installing or operating the Flowmeter.
CAUTION
Inspect the Flowmeter for visual damage before use, DO NOT USE if damaged.
NOTE: Precision Medical, Inc. strongly recommends the use of kink proof cannula.

1. Turn Knob to the “OFF” position.

2. Connect the Flowmeter to the appropriate gas source. The appropriate gas and pressure are specified on the Flow Tube or Flowmeter body.

3. Verify that the Float Ball is at the very bottom of the Flow Tube.
   NOTE: If the Float is not resting at the bottom of the Flow Tube, the product is leaking; consult the “TROUBLESHOOTING” Guide.

4. Adjust Flow:
   To increase – Turn Knob counterclockwise
   To decrease – Turn Knob clockwise

5. Set flow by aligning center of Float Ball with indicator lines on the Flow Tube.

6. Adjusting flow beyond the last calibrated indicator line will result in an undetermined flow.

7. To obtain maximum flush flow, turn Knob fully Counterclockwise.
   NOTE: Flush flow is any flow above the last calibrated line on the Flow Tube with an unrestricted flow, as indicated on flowmeter labeling.

Applies to 1MFA and 8MFA Series MRI labeled Flowmeters only!
Indicates the device is MR Conditional and can be used in an MR Environment
WARNING! This product may be used near a MR Environment (e.g. in the MR System room near the scanner). It should not be utilized directly inside of the MR System (e.g. inside of the bore of the scanner). The device must be securely attached to a wall Gas Outlet.

• This information must be kept with the device.
• MRI Conditional with 1.5T MR systems.
• Service must be performed by qualified personnel.
• Flow meters must be kept to manufacturing specifications.
• Fittings must be kept MR conditional if serviced or replaced.
• MRI manufactures guidelines supersedes this information
• Consult MRI Manufacture if used with an Open MRI.

LIMITED WARRANTY AND LIMITATION OF LIABILITY

Precision Medical, Inc. warrants that the Medical Gas Flowmeter (the Product) will be free of defects in workmanship and/or material for the following period:
(a) Flow Tube and Housing Lifetime of the product
(b) Needle Valve Five (5) years from shipment
(c) All other parts of the Medical One (1) year from shipment Gas Flowmeter not identified in (a) or (b) above
Warranty does not cover breakage / abuse.
Should any failure to conform to this warranty appear within the applicable period, Precision Medical, Inc. shall, upon written notification thereof and substantiation that the goods have been stored, installed, maintained and operated in accordance with Precision Medical, Inc.’s instructions and standard industry practice, and that no modifications, substitutions, or alterations have been made to the goods, correct suchdefect by suitable repair or replacement at its own expense.
ORAL STATEMENTS DO NOT CONSTITUTE WARRANTIES.
The representative of Precision Medical, Inc. or any retailers are not authorized to make oral warranties about the merchandise described in this contract, and any such statements shall not be relied upon and are not part of the contract for sale. Thus, this writing is a final, complete and exclusive statement of the terms of that contract.
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ANY WARRANTY OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE OR OTHER WARRANTY OF QUALITY, WHETHER EXPRESS OR IMPLIED.
Precision Medical, Inc. shall not under any circumstances be liable for special, incidental or consequential damages including but not limited to lost profits, lost sales, or injury to person or property. Correction of non- conformities as provided above shall constitute fulfillment of all liabilities of Precision Medical, Inc. whether based on contract, negligence, strict tort or otherwise. Precision Medical, Inc. reserves the right to discontinue manufacture of any product or change product materials, designs, or specifications without notice. Precision Medical, Inc. reserves the right to correct clerical or typographical errors without penalty.

300 Held Drive
Northampton PA 18067, USA
www.precisionmedical.com
T: (+001)610-262-6090 • F: (+001) 610-262-6080
ISO 13485 Certified
2460
For Declaration of Conformity and Replacement Parts List, refer to the Flowmeter product page on our website.
Emergo Europe B.V.
Prinsessegracht 20
2514 AP The Hague
The Netherlands

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