Fisher & Paykel MR810 User Manual

MANUFACTURER Fisher & Paykel Healthcare Ltd, 15 Maurice Paykel Place, East Tamaki, Auckland 2013, PO Box 14 348 Panmure, Auckland 1741, New Zealand Tel: [phone] Fax: [phone] Email:
[e-mail] Web: www.fphcare.com AUSTRALIA Fisher & Paykel Healthcare Pty Limited, 36-40 New Street, PO Box 167, Ringwood, Melbourne, Victoria 3134, Australia Tel:[phone] Fax:[phone]
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8 36 63 10 SWITZERLAND Tel: [phone] Fax: [phone] TAIWAN Tel:[phone] Fax:[phone] T URKEY Fisher Paykel Sağlık Ürünleri Ticaret Limited Şirketi, Alinteri Bulvari 1161/1 Sokak No. 12-

14, P.O. Box 06371 Ostim, Ankara, Turkey Tel: [phone] Fax: [phone] UK

Fisher & Paykel Healthcare Ltd, Unit 16, Cordwallis Park, Clivemont Road, Maidenhead, Berkshire SL6 7BU, UK

Tel:[phone] Fax:[phone] U SA/CANADA Tel: [phone] or [phone] Fax:[phone]

SPECIFICATIONS

Breathing Circuit

Setting

Patient interface temperature (°C)

Flow range 5-20 L/Min

Flow range 5-60 L/Min

900MR810/

900MR810E

Low

28 to 29

28 to 29

Medium

28 to 30

28 to 31

High

31 to 32

30 to 32

Type BF

Applied

Part

ATTENTION

Consult

accompanying

documents

Alternating

current

Resistant
to vertical

falling drips

Caution

– Hot

surface

Equipotential

Stud

Date of

manufacture

Respiratory Humidifier Classified by

Underwriters Laboratories Inc.

with respect to electric shock, fire

and mechanical hazards only

in accordance with UL 60601-1 and

CAN/CSA C22.2 No. 601.1 84DJ

WARNING:

 The MR810 does not deliver body temperature saturated gases

and is therefore not recommended for 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 “hospital grade” receptacle.

 Ensure that the humidifier is always positioned lower than the

patient’s airway.

 Ensure the humidifier is securely mounted.
 DO NOT use for flow ˂5 L/min.
 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.

 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 for Personal
Computers.

 This device is not suitable for use in the presence of

flammable anaesthetic mixes or nitrous oxide.

 Remove any sources of ignition: such as cigarettes, an open

flame, or materials which burn or ignite easily ay high oxygen
concentrations.

 Keep oxygen regulators, cylinder valves, tubing connections

and all other oxygen equipment away from oil, grease, or
greasy substances. Spontaneous and violent ignition may
occur if these substances come into contact with oxygen
under pressure.

 Visually inspect equipment for damage before use.
 Hot surfaces may exceed 75 °

TRANSPORT & STORAGE:

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

OPERATING CONDITIONS

Recommended ambient temperature: 18 to 26 °C.
Humidity Performance: > 10 mg/L, 5 L/min < flow < 60 L/min.
Warm-up Time: < 60 minutes.

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 of
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.

DISPOSAL INSTRUCTIONS:

MR810 Disposal Instructions

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

CLEANING:

The MR810 Respiratory Humidifier is a multiple patient, multiple reuse device.
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).

Fragile

Serial

Port

Respiratory Humidifier Classified by

Underwriters Laboratories Inc.

with respect to electric shock, fire

and mechanical hazards only

in accordance with UL 60601-1 and

CAN/CSA C22.2 No. 601.1 84DJ

Size: 94 mm x 154 x 135, Weight 1.7 kg (no chamber fitted), 2.0 kg (chamber fitted and filled with
water). Electrical Classification: CLASS 1, TYPE BF, IPX1

ELECTRICAL RATINGS:

Supply frequency: 60 Hz, Voltage: 115 V~, Current: 1.6 A max at 115 V~
Power Input: 200 VA, Heater plate: 150 W.
Heater wire: 22 V~, 1.36 A, 30 W, 60 Hz
Heater plate over-temperature cutout 93 ± 6 °C
IEC 60601-1 Classification Class 1

Representative Performance (Heater wire mode) (at 22°C ambient)

SYMBOL DEFINITIONS:

3. HEATER WIRE MODE (ie. 900MR810/900MR810E CIRCUIT)
Insert heater wire adaptor to circuit (C). See “Heater Wire Mode Indicator”.

Note: Remove scrolls from scrolled chambers.

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

Indications for Use:

The Fisher & Paykel MR810
System is intended to provide
therapeutic levels of heat and
humidity to a patient’s inspired
respiratory gases, when using a
continuous or intermittent non­invasive ventilator system or a
continuous gas flow system.
The MR810 System is intended
for non-invasive therapies only.
Addition of heat and humidity to
the supply of cold and dry
respiratory gases provided
through non-invasive ventilation is
beneficial to prevent drying of the
patient airways.
The MR810 System is designed
for use in hospitals, long term care
facilities and homes under the
prescription of a qualified medical
professional.

INSTRUCTION

SHEET DO NOT

DISCARD

REF 185042330 Rev C

US 2014-03

PLEASE READ OPERATING INSTRUCTION WARNINGS
BEFORE SETTING UP THE MR810

SET UP

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 and to the air entrainer, as required (D). Connect to patient interface (G).

RESPIRATORY HUMIDIFIER

A

B

C

D

E F G

WARNING: Ensure that probe

port caps are inserted into the
circuit.

A

OPERATION

Power Button

Pressing this button turns the humidifier on or off (stand by).

Note: The MR810 defaults to HIGH when turned on.

Temperature & Humidity Control
Button & Indicator

Pressing this button cycles the humidifier setting
between low, medium, and high.

Temperature & Humidity
Settings

Low
Medium
High

Note: For maximum humidity
delivery use the high setting.

See Manual Indicator
Humidifier Faulty

If the red light is illuminated, the humidifier and all
accessories should be immediately removed and sent
for servicing.

Heater Wire Mode Indicator

If the green light is illuminated, the heater wire is
correctly connected to the heater wire circuit.

If the green light is off while connected to the heater
wire circuit, there may be a fault with the heater
wire circuit or heater base.

If not connected to a heater wire circuit, non-heater
wire mode is initiated.

C

Ambient Temperature Sensor

Monitors air temperature and adjusts the
heater wire power to minimize breathing
circuit condensate. Keep away from
drafts and heat.