IWorX IWire ROAM Wireless Bedienungsanleitung

iWire ROAM Wireless

iWire ROAM Wireless Manual

Expand your iWorx TA or RA system with wireless recordings. The iWire ROAM Wireless is a

versatile, wireless system designed to provide long-term recording and unrestricted movement. The

recording device easily attaches to the su ject with standard electrodes. The protective case dou les as

a charging station. The system works with iWorx Recorders with an iWire interface. Data can e

quickly analyzed with the included La Scri e analysis software or exported directly for other

processing. The iWire ROAM Wireless allows for hours of continuous recording with an untethered

reach of 20 feet.

Equipment

The list elow indicates all the products included. If you find any missing items please notify iWorx

Systems as soon as possi le.

iWire ROAM Wireless Peripheral

Charger Box

iWire Receiver Dongle

USB charging ca le

Disposa le Electrodes

*Head and - included with the EEG recording system only

Specifications

Device Channels

IWireR-ECG 1 ECG channel,

1 Respiration Channel

IWireR-ECGA 1 ECG channel,

1 Respiration Channel,

3-axis Accelerometer

IWireR-B1 2 ECG/EMG channels

IWireR-B1A 2 ECG/EMG channels

3-axis Accelerometer

IWireR-B2 2 ECG/EMG channels

IWireR-B2A 2 ECG/EMG channels

3-axis Accelerometer

iWire ROAM Wireless

Specifications for all iWire Roam Devices

Battery capacity 11 mAhr

Battery life > 8hrs

Charging case power requirements Provided USB cable to computer

Range upto 2 ft

Sampling Speed 5k samples per sec. aggregate

Resolution < 6 µV

Weight 16.8g

Dimensions 44.2mm x 42.7mm

Protection against electric shock (IEC 6 6 1-1) Charging Case - Class II, continuous operation

ROAM peripheral - Internally powered,

continuous operation, type BF applied part

Charging the Device

1. The ROAM case is designed to charge the

device. Be sure that the iWire ROAM

Wireless device (the part with the iWorx logo

and serial num er) is secure in the case.

2. Take the provided charger ca le and connect

one end to the USB port of your computer.

3. Connect the other side of the charger ca le to

the port located on the front of the case.

4. If done correctly, a light will illuminate on the

iWire ROAM Wireless device. A red light indicates that the unit is charging. A green light

indicates a full attery. It takes approximately two hours for complete charging.

5. Please charge the device efore each use. In storage, the device goes to sleep to conserve

energy, ut it is still using power to monitor the accelerator, so that it can e woken up when

needed.

Device Set Up

1. Remove the iWire ROAM Wireless device from the charging ox. Plug the iWire receiver

dongle into your iWorx TA or RA.

◦The LED on the receiver will link green while it looks for the transmitter. Once the

transmitter is found, the light will stay solid green to show that the connection has een

made. Move the iWire ROAM device transmitter or tap the transmitter if receiver dongle

doesn’t convert to solid green light.

◦Choose the applica le experiment in la scri e. If it is not there then ensure you have the

latest version of La Scri e installed and re-load the settings group.

iWire ROAM Wireless

Loading Setting roup

1. Open La Scri e.

2. Click Settings → Load Group.

If using the TA – Choose Complete Settings → scroll to the ottom and select

IPLMv7Complete.iwxgrp and click “Open”.

If using the RA - Choose Research Settings → Choose your equipment from the list.

Choose the group you wish to load and click “Open”.

3. The window will close and you will e ack to the original La Scri e recording window.

4. Select the desired experiment, a pdf of the experiment and a La Scri e window with the correct

settings should open.

5. All Experiments will include specific instructions for connections to the su ject.

eneral Safety Tips for using the peripheral

WARNING: Do not attempt to service. Any repair will e made y iWorx Systems, Inc.

Do not use if there are any signs of damage.

Do not touch the charging ase and the su ject simultaneously.

Only use provided charging ca le with a computer.

iWire ROAM Wireless

Consumables

The silver-silver chloride electrodes are the part of the instrument that is in contact with the skin y

making electrical contact etween the skin and the sensor. Silver-silver chloride electrodes are the est

electrodes for recording EMG signals. The electrodes are disposa le and should e replaced after each

use.

iWorx offers three types of silver-silver chloride electrodes differing ased on the width of the adhesive

material and position of the electrode in it.

Picture Description (click part number to go to

website)

A-GC-7165

Foam solid gel electrodes

50 x 54mm

150 per package

A-GC-7165P

Pediatric foam solid gel electrodes

3 mm

15 per package

A-ELEC-E-30

Foam solid gel electrodes

35 / 53mm

Latex and PVC free

Diaphoretic / Hypoallergenic

Proper skin preparation is important to get a good signal and avoid artifacts.

•Before applying electrodes, make sure the skin surface is clean and dry:

•A rade the skin with an a rasive cream, such as NuPrep, to remove dead skin.

•Alternatively, you can also clean skin with an alcohol wipe and let it dry, ut this is not as

efficient as the a rasive cream.

Tip: It is easier to connect the electrodes to the snap cable before placing the electrode on the

subject.

iWire ROAM Wireless

Warranty Information:

No modification of this equipment is allowed. The unit contains no customer servicea le parts. If a

pro lem occurs, contact your iWorx representative. Repair, if required, will e completed at iWorx

Systems, Inc. The unit is protected y a 3-year warranty, and if the product is opened y any one other

than iWorx personnel the warranty will e void.

Cleaning

The ROAM unit may e wiped down with a dry lint free cloth.

*If using the EEG system the head and may e cleaned with an alcohol wipe.

Intended Usage

iWorx Systems Inc. instruments, components, and accessories are designed for educational and

research oriented life science applications and investigations. iWorx Systems Inc. does not condone the

use of its instruments for clinical medical applications. Instruments, components, and accessories

provided y iWorx Systems Inc. are not intended for the diagnosis, cure, mitigation, treatment, or

prevention of disease.

Furthermore, the unit is intended for research and teaching applications. The fact the this product is

IEC 60601-1 compliant in no way means that it is to e used for medical purposes. It was tested to the

60601-1 standard ecause it’s a more rigorous form of testing.

Intended Environment:

The unit should only e used in a classroom or la oratory setting.

Storage Conditions:

•Temperature - 0°C to 40°C

•Humidity - 0 to 70%

Operating Conditions:

•Temperature - 10°C to 30°C.

•Humidity - 0 to 60%

Disposal:

The user has two options, either send it ack to the manufacturer or send to a recycling center.

iWire ROAM Wireless

Explanation of Symbols:

Class II Electrical Equipment

Additional safety measures against electric shock have een implemented.

Type BF Applied Part

Input connectors are suita le for connection to humans provided there is no direct

electrical connection to the heart and provides additional protection against electric shock.

CE Mark

The equipment meets the appropriate EU directives.

Company Information:

Headquarters

iWorx Systems, Inc.

62 Littleworth Road

Dover, NH 03820

Phone: (800) 234-1757

Fax: (603) 742-2455

Website: www.iWorx.com

iWire ROAM Wireless

Supplier's Declaration of Conformity for FCC

7 CFR § 2.1077 Compliance Information

Unique Identifier: IXR-ECG, IXR-ECGA, IXR-B1, IXR-B1A, IXR-B2, IXR-B2A, iWireR-ECG,

iWireR-ECGA, iWireR-B1, iWireR-B1A, iWireR-B2, iWireR-B2A

Responsible Party – U.S. Contact Information

iWorx Systems Inc

62 Littleworth Road

Dover, NH 03820

Telephone number : +1-603-742-2492

Internet contact information : https://iworx.com

FCC Compliance Statement (e.g., products su ject to Part 15)

This device complies with Part 15 of the FCC Rules. Operatio is subject to the followi g two

co ditio s: (1) This device may ot cause harmful i terfere ce, a d (2) this device must

accept a y i terfere ce received, i cludi g i terfere ce that may cause u desired operatio .

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