Respironics WristOx Bedienungsanleitung

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Operator’s Manual

Wrist Oximeter

WristOx

TM

English

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

WARNING! Read this entire manual carefully before using the WristOx.

The information in this manual has been checked carefully and is believed to be accurate. In the interest

of continued product development, Respironics reserves the right to make changes and improvements to

this manual and the products it describes at any time, without notice or obligation.

References to “Respironics” in this manual imply Respironics, Inc. Respironics is a registered

trademark of Respironics, Inc. References to “NONIN” in this manual imply Nonin Medical, Inc.

Nonin is a registered trademark of Nonin Medical, Inc. WristOx™ is a trademark of Nonin Medical, Inc.

©2004 Respironics

Respironics Phone: 800-345-6443

1001 Murry Ridge Lane Website: www.respironics.com

Murrysville, Pennsylvania 15668-8550 USA

5

Guide to Symbols

Detailed information for functional symbols can be found in “Using the WristOx.”

Symbol Description

Attention: See Instructions for Use or related materials.

Type BF Applied Part

(Patient isolation from electrical shock).

UL Mark for Canada and the United States with respect to

electric shock, fire, and mechanical hazards only in accordance with

UL 2601-1 and CAN/CSA C22.1 No. 601.1.

!

C

L

A

S

S

I

F

I

E

D

US

CUL

6

Serial Number

Detailed information for functional symbols can be found in “Using the WristOx.”

Symbol Description

SN

7

Precautions for Use

Read and follow all safety instructions before using the WristOx.

Contraindications

• Do not use the WristOx in a magnetic resonance imaging (MRI) environment.

• Explosion Hazard: Do not use the WristOx in an explosive atmosphere or in the presence

of flammable anesthetics or gases.

Warnings

• Read this entire manual carefully before using the WristOx.

• The WristOx is intended only as an adjunct in patient assessment. It must be used in con-

junction with other methods of assessing clinical signs and symptoms.

• General operation of the WristOx might be affected by the presence of an electrosurgical

unit (ESU).

8

• As with all medical equipment, carefully route patient cables and connections to reduce the

possibility of patient entanglement or strangulation.

• Use the WristOx only within the specified temperature ranges: +32°F to +122°F (0°C to

50°C) for operating, and 14°F to 122°F (-10°C to +50°C) for storage and transportation.

• Use only Respironics-manufactured pulse oximeter sensors. These sensors are manufac-

tured to meet the accuracy specifications for Respironics pulse oximeters. Using other

manufacturers’ sensors can result in improper pulse oximeter performance.

• Discontinue use of adhesive tape strips if the patient exhibits an allergic reaction to the

adhesive material.

• Do not stretch the adhesive tape while applying the pulse oximeter sensor.

• Ensure that the wrist band fits comfortably on the patient’s arm. Do not over-tighten the

wrist band.

• Pulse oximeter readings might be affected while patients are being defibrillated.

9

Cautions

• U.S. federal law restricts this device to sale by or on the order of a physician.

• Before using any sensor, carefully read the Directions for Use.

• Do not, under any circumstances, perform any testing or maintenance on the WristOx

while it is being used to monitor a patient.

• Verify that all visible indicators appear during the start-up (initialization) sequence. If any

indicator does not appear, do not use the WristOx. Contact Respironics Customer Service

for assistance.

• This equipment complies with International Standard EN 60601-1-2:2001 for electromag-

netic compatibility for medical electrical equipment and/or systems. This standard is

designed to provide reasonable protection against harmful interference in a typical medical

installation. However, because of the proliferation of radio-frequency transmitting equip-

ment and other sources of electrical noise in healthcare and other environments (for exam-

ple, cellular phones, mobile two-way radios, electrical appliances), it is possible that high

10

levels of such interference due to close proximity or strength of a source might disrupt the

performance of this device.

• If the WristOx fails to respond as described, refer to “Troubleshooting” or discontinue use

until the situation has been corrected by qualified personnel.

• Do not remove any covers other than the battery cover when replacing batteries. There are

no user-serviceable parts inside.

• Batteries might leak or explode if used or disposed of improperly.

• Follow local governing ordinances and recycling instructions regarding disposal or recy-

cling of the device and device components, including batteries.

• Do not immerse the WristOx or sensors in water or any other liquids.

• Do not place or pour liquids on top of the WristOx.

• The WristOx is a precision electronic instrument. It must be repaired by trained

Respironics personnel only.