Fisher Paykel 900mr860 Temperature Probe Instructions

FISHER PAYKEL 900MR860 Temperature Probe

USER INSTRUCTIONS

Reprocessing Diagram

E.g.

• Tuffie 5 Wipes
• Tristel Wipes System
• Metrex Caviwipes 1
• Metrex Caviwipes
• PDI Sani-Cloth AF3
• PDI Super Sani-Cloth
• Clorox Hydrogen Peroxide

e.g. STERIS Revital-Ox Resert HLD, 2.0 – 4.0% glutaraldehyde (e.g. Cidex, Metricide, ProCide-D), 0.95% glutaraldehyde/1.64% phenol
(e.g. Sporicidin), 0.55% ortho‑phthalaldehyde (e.g. Cidex OPA), 7.5% hydrogen peroxide (e.g. Sporox).

Setup Diagram

Temperature Probe User Instructions

Intended Use:
The Temperature Probe is designed for measuring gas temperature and flow with Fisher & Paykel Healthcare MR850 and HC550 Humidifiers and Fisher & Paykel Healthcare Breathing Circuits.

Specification:

Expected Service Life:
3 years, if used in accordance with this User Instruction. Note: Service life may vary depending on usage pattern.

Setup:
Refer to the setup diagram.

1. Before use remove and discard Protective Sleeve D, if present, from Chamber Probe B .
2. Visually inspect entire product for damage before use. Discard if damaged.
3. Push the Airway Probe A and Chamber Probe B into the Breathing Circuit making sure they are correctly located and pushed into place.
4. The probe lead can be restrained using
   Breathing Circuit Clips.
   1. If patient is in an incubator, refer to Breathing Circuit User Instructions for probe positioning information.
5. Insert the Temperature Probe Connector C into the blue socket on the Humidifier.
6. Perform ventilator leak test on the Breathing Circuit before use.

Maintenance:
Probe maintenance and accuracy checks should be routinely performed. For further information, refer to the MR850 or HC550 Technical Manual (available from your local Fisher & Paykel Healthcare representative).

Reprocessing:
The following parts are in contact with the gas path and can become contaminated with body fluids or expired gases:

Airway Probe A, Chamber Probe B.
Recommended cleaning procedures between uses (refer to reprocessing diagram):

1. Remove any visible soil using a soft bristle brush, water and a mild non-abrasive detergent.
   Do not immerse the Temperature Probe Connector C in any liquid.
2. Rinse in water after cleaning.
3. Dry with a non-shedding cloth.
4. Check for visible signs of damage. Discard if damaged. Repeat the cleaning steps if parts are not visually clean.
5. Proceed to either step A, B, C or D depending on hospital guidelines.
   • A. MANUAL DISINFECTION – WIPES
     1.  Follow the wiping instructions supplied by the manufacturer.
     2. Check for visible signs of damage.
        Discard if damaged.
     3. If applicable, product can be packaged for reuse.
   • B. MANUAL DISINFECTION – CHEMICAL
     1. Follow the soaking instructions supplied by the manufacturer of the disinfection solution.
        Do not immerse the Temperature
        Probe Connector C in any liquid.
        Cover container while soaking.
     2. Rinse in water after chemical soaking.
     3. Dry with a non-shedding cloth.
     4. Check for visible signs of damage.
        Discard if damaged.
     5. If applicable, product can be packaged for reuse.
   • C. VAPORISED HYDROGEN PEROXIDE (VHP) STERILIZATION
     1. Follow hospital guidelines for using the equipment (Equipment) and settings (Setting).
   • D. ETHYLENE OXIDE (ETO) STERILIZATION
     1. Follow hospital guidelines for process.
     2. Allow at least 12 hours aeration.
6. Store as per hospital guidelines.

Notes:

• Fisher & Paykel Healthcare do not recommend exceeding the number of reprocessing cycles stated (Reprocessing Cycles).
• The product is not designed for autoclave sterilization processes.
• Follow these recommended cleaning procedures and the user instructions of the cleaning agents or disinfection/sterilization equipment. It is the user’s responsibility to qualify any deviations from these procedures, both for disinfecting efficacy and physical effect.

Warnings:

• The use of breathing circuits, chambers, other accessories or parts which are not approved by Fisher & Paykel Healthcare may impair performance or compromise safety.
• Failure to perform routine probe accuracy and visible damage checks may impair performance or compromise safety.
• Ensure that both Temperature Probe sensors are correctly and securely fitted. Failure to do so may result in gas temperatures in excess of 41 °C being delivered to the patient.
• Do not touch the glass tip of the Chamber
  Probe B during use; it may cause a skin burn.
• Gas mixes, such as helium-oxygen mixtures, that have different physical or thermal properties than air or air-oxygen mixture, may impair system performance or compromise safety.
• No automated method for cleaning and disinfection is recommended.
• California residents please be advised of the following, pursuant to Proposition 65:
  This product contains chemicals known to the State of California to cause cancer,birth defects and other reproductive harm.
  For more information, please visit: www.fphcare.com/prop65.

Disposal:
Dispose according to standard hospital guidelines for electrical and electronic equipment.

Symbol Definition:

	Operating Instructions
	Date of manufacture
	Manufacturer
	Dispose of product in correct manner
	Transportation and storage humidity limitation
	Transportation and storage temperature limitation
	Lot number
	Reference number
	European union authorised representative
	Prescription only
	CE Marking 93/42/EEC
	MD symbol

Manufacturer Fisher & Paykel Healthcare Ltd, 15 Maurice Paykel Place, East Tamaki, Auckland 2013, PO Box 14 348 Panmure, Auckland 1741, New Zealand Tel: +64 9 574 0100
Fax: +64 9 574 0158
Email: [email protected]
Web: www.fphcare.com Importer/ Distributor

REF 617135 REV E 2022-02 © 2022 Fisher & Paykel Healthcare Limited

References

• Quality & Regulatory | Fisher & Paykel Healthcare
• Home | Fisher & Paykel Healthcare