810 RESPIRATORY HUMIDIFIER

SPECIFICATIONS

Size: 94 mm x 154 x 135 mm. Weight: 1.7 kg (no chamber fitted), 2.0 kg (chamber fitted and filled with water).

Electrical Ratings

• Supply frequency: 50 or 60 Hz
• Voltage: 230 V~
• Current: 0.8 A max at 230 V~
• Heater plate: 150 W
• Heater wire: 22 V~, 1.36 A, 30 W, 50 or 60 Hz
• Heater plate over-temperature cutout: 93 ± 6 °C
• IEC 60601-1 Classification: Class I, Type BF, IPX1

Performance (at 23 °C Ambient Temperature)

CAUTION: MR810 does not deliver body temperature saturated gases.

Humidity Performance: > 10 mg/L, 5 L/min < flow < 60 L/min. DO NOT use for flow < 5 L/min.

Warm-up Time: < 60 minutes.

Symbol Definitions

⚠️ Hot Surface

? Resistant to vertical falling drips

⚡ Equipotential Stud

? Serial Port

✅ Regulatory Compliance Mark

~ Alternating Current

⚕️ Type BF Applied Part

? ATTENTION Consult accompanying documents

? Fragile, handle with care

? Date of Manufacture

WARNING

• Caution is required when delivering gases that are not body temperature saturated, to patients with bypassed airways.
• The use of breathing circuits, chambers, or other accessories which are NOT approved by Fisher & Paykel Healthcare, may impair performance or compromise safety.
• Refer to operating instructions for each accessory.
• Ensure maintenance of grounding integrity by connecting to an appropriately grounded receptacle.
• Ensure that the humidifier is always positioned lower than the patient's airway.
• Ensure the humidifier is securely mounted.
• The operation of high frequency surgical apparatus, short wave or microwave equipment in the vicinity of the humidifier may adversely affect its function. If this occurs the humidifier should be removed from the vicinity of such devices.
• Visually inspect equipment for damage before use.
• Hot surfaces may exceed 75 °C.
• The serial port must not be used when the humidifier is in patient use. Equipment connected to the serial port must comply with the safety standard IEC60950.
• This device is designed for the delivery of air, oxygen and/or nitrous oxide. It is not suitable for the delivery of flammable anaesthetic gas mixes.
• Remove any sources of ignition: such as cigarettes, an open flame, or materials which burn or ignite easily at high oxygen concentrations.

Required Accessories

• Humidifier Chamber (e.g.: MR290)
• Breathing Circuit: (e.g.: 'Evatherm' 900MR810(E), RT308 / RT307)
• Mounting Bracket (to suit ventilator)

Choice will depend on application. Please contact your local F&P Healthcare representative for recommendations.

SET UP

PLEASE READ OPERATING INSTRUCTION WARNINGS BEFORE SETTING UP THE MR810

1. Slide humidification chamber (B) onto humidifier base (A) and connect breathing circuit (F) (refer to humidification chamber and breathing circuit operating instructions for further details). Hang the waterbag from a waterbag pole (E).
2. Connect oxygen tubing to the O2 flow meter (not included in the 900MR810(E) / RT308 / RT307 kits) to the air entrainer (D). Connect to patient interface (G).

3. 3a. HEATER WIRE MODE (i.e. 900MR810 / 900MR810E / RT308 CIRCUIT)

   Insert heater wire adaptor to circuit (C). See "Heater Wire Mode Indicator".

4. 3b. NON-HEATER WIRE MODE RT307 CIRCUIT

   Secure heater wire adaptor to the power cable (C).

Diagram Description: The diagram shows the MR810 humidifier system components labeled A through G. A is the humidifier base, B is the humidification chamber, C is the heater wire adaptor/power cable connection, D is the air entrainer, E is the waterbag pole, F is the breathing circuit, and G is the patient interface. Arrows indicate connection points.

4. The humidification system is now set up and ready for use. For maximum humidity delivery use the high setting. For other applications contact your local Fisher & Paykel Healthcare representative.

Note: Remove scrolls from scrolled chambers.

The MR810 respiratory humidifier warms and humidifies gases delivered to patients requiring noninvasive and/or constant flow applications.

INSTRUCTION SHEET DO NOT DISCARD

WARNING: When using RT series circuits, ensure that probe port caps are inserted into the circuit.

TRANSPORT & STORAGE

Temperature: -10 to 50 °C (14 to 122 °F)

OPERATING CONDITIONS

• Recommended ambient temperature: 18 to 28 °C (64 to 82 °F)
• Humidity: 10 to 95% RH
• Mode of operation: Continuous

CLEANING

The humidifier base and heater wire adaptor can be cleaned when required with a damp cloth using a mild non-abrasive cleaning solution. (Refer to the MR810 technical manual for a list of approved cleaning agents).

ROUTINE MAINTENANCE AND SERVICING

Refer maintenance and servicing to qualified service personnel. A full technical description including annual maintenance and service data is contained in the Technical Manual which is available from your supplier or Fisher & Paykel Healthcare (REF 185042601).

DEVICE AND CONSUMABLE DISPOSAL

MR810 Disposal Instructions

This device contains electronics. Please do not discard as regular rubbish. Dispose of electronics according to local guidelines.

Consumable Disposal Instructions

Place the breathing tube and water chamber in a rubbish bag at the end of use and discard according to hospital protocol.

DIAGNOSTIC PORT

The diagnostic port is not intended for use during operation - Factory use only.

ELECTROMAGNETIC COMPATIBILITY

The device complies with the electromagnetic compatibility requirements of IEC60601-1-2. A full technical report is contained in the Technical Manual available from your supplier or Fisher & Paykel Healthcare (REF 185042601). In certain circumstances the device may affect or be affected by nearby portable mobile radio frequency communication equipment, due to the effects of electromagnetic interference. If this should happen, try moving your device or the location of the equipment causing interference, or alternatively consult your healthcare provider.

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: info@fphcare.co.nz Web: www.fphcare.com

Regional Contacts:

• AUSTRALIA: Fisher & Paykel Healthcare Pty Limited, 36-40 New Street, PO Box 167, Ringwood, Melbourne, Victoria 3134, Australia. Tel:+61 3 9879 5022 Fax:+61 3 9879 5232
• AUSTRIA: Tel: 0800 29 31 23 Fax: 0800 29 31 22
• BENELUX: Tel:+31 40 216 3555 Fax:+31 40 216 3554
• BRAZIL: Fisher & Paykel do Brasil, Rua Sampaio Viana, 277 cj 21, Paraíso, 04004-000, São Paulo - SP, Brazil. Tel: +55 11 2548 8002
• CHINA: 费雪派克医疗保健(广州)有限公司, 广州高新技术产业开发区科学城科丰路31号G12栋301号. Tel:+86 20 32053486 Fax:+86 20 32052132
• FINLAND: Tel:+358 (0)405 406618 Fax:+46 (0)8 36 6310
• FRANCE: Tel:+33 1 6446 5201 Fax:+33 1 6446 5221
• GERMANY: Tel:+49 7181 98599 0 Fax:+49 7181 98599 66
• INDIA: Tel:+91 80 4284 4000 Fax:+91 80 4123 6044
• IRISH REPUBLIC: Tel: 1800 409 011
• ITALY: Tel:+39 06 7839 2939 Fax:+39 06 7814 7709
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• SWITZERLAND: Tel: 0800 83 47 63 Fax: 0800 83 47 54
• TAIWAN: Tel:+886 2 8751 1739 Fax:+886 2 8751 5625
• TURKEY: Fisher Paykel Sağlık Ürünleri Ticaret Limited Şirketi, Alinteri Bulvarı 1161/1 Sokak No. 12-14, P.O. Box 06371 Ostim, Ankara, Turkey. Tel: +90 312 354 34 12 Fax: +90 312 354 31 01
• UK EC REP: Fisher & Paykel Healthcare Ltd, Unit 16, Cordwallis Park, Clivemont Road, Maidenhead, Berkshire SL6 7BU, UK. Tel:+44 1628 626 136 Fax:+44 1628 626 146
• USA/CANADA: Tel: 1800 446 3908 or +1 949 453 4000 Fax:+1 949 453 4001

OPERATION