Shaded boxes draw attention to contraindications, warnings, cautions
and notes.
The boxed messages are important. Be sure to read them.
The information in this manual has been carefully checked and is
believed to be accurate. In the interest of continued product
development, RESPIRONICS, INC. reserves the right to make
changes and improvements in this manual and the products it
describes at any time, without notice or obligation.
Caution: Federal Law (USA) restricts this device to sale by or on the
order of a physician.
Respironics Georgia
175 Chastain Meadows Court
Kennesaw, Georgia 30144-3724
USA
Telephone: 1-770-499-1212
Fax: 1-770-499-0117
Customer Service Telephone: 1-800-345-6443 (USA and Canada)
Customer Service Fax: 1-800-886-0245 (USA and Canada)
www.respironics.com
Type BF Applied Part:
(Patient isolation from electrical shock).
Canadian Standards Association
Meets both Canadian and United States
Standards.
CE Marking indicating conformance to EC
directive No. 93/42/EEC concerning medical
devices.
Not for Continuous Monitoring
(No Alarm for SpO2)
vi
Contraindications, Warnings, and Cautions
Do not use the 950 in an MRI environment.
Do not operate the 950 in an explosive atmosphere.
Do not use the 950 on infant or neonatal patients.
Batteries may leak or explode if used or disposed of improperly.
Federal Law (USA) restricts this device to sale by or on the order
of a physician.
Read this entire manual carefully before using the Respironics 950
Pulse Oximeter.
The 950 determines the percentage of arterial oxygen saturation of
functional hemoglobin. Significant levels of dysfunctional
hemoglobin such as carboxyhemoglobin or methemoglobin may
affect the accuracy of the measurement.
Cardiogreen and other intravascular dyes, depending on the
concentration, may affect SpO2 accuracy.
The 950 must be able to measure the pulse properly to obtain
accurate SpO2 measurement. Verify that nothing is hindering the
pulse measurement before relying on the SpO2 measurement.
Some situations that may contribute to erroneous pulse
measurement are:
• inadequate perfusion,
• excessive patient movement,
• pulse oximeter and blood pressure measurement on the
The 950 may interpret motion artifact of sufficient amplitude and
regularity as good perfusion (green).
Do not use the 950 in situations where alarms are required. The
950 has no audible alarms.
The 950 is intended for spot-checking or continuous monitoring by
an attending health care professional. Because the 950 has no
audible alarms, international labeling requirements (ISO 9919)
dictate it be labeled, “Not for continuous monitoring”.
CONTRAINDICATIONS:
WARNINGS:
CAUTIONS:
same limb, etc.
English
1
CAUTIONS:(Continued)
Check application site periodically (at least every thirty minutes) to
determine circulation, positioning and skin sensitivity.
The 950 may not work for all patients. If you are unable to achieve
stable readings, discontinue use.
Finger nail polish may reduce light transmission and thereby affect
SpO2 accuracy.
A flexible circuit connects the two halves of the 950. Do not twist or
pull on the connection.
Do not use different types of batteries at the same time. Do not mix
fully charged and partially charged cells at the same time. These
actions may cause the batteries to leak.
Batteries must be removed if the 950 is going to be stored for more
than one month or batteries may leak.
Do not immerse the 950 in liquid to clean.
2
Introduction
Description
Respironics, Inc. has integrated the finger clip sensor and the
electronics of the Respironics Model 920 hand held Pulse Oximeter
into one unit, the Model 950. The 950 is very small (1.3 inch W x 1.3
inch H x 2.2 inch L) and lightweight (2 ounces).
The 950 displays numerical values for functional arterial hemoglobin
oxygen saturation (%SpO2) in percentage and pulse rate (
beats per minute on light emitting diode (LED) digital displays.
With each detected pulse, the Perfusion Display blinks. Patient
perfusion signals are graded as good, marginal or inadequate and are
indicated as such by the perfusion indicator changing color from green
to yellow or red respectively. This sophisticated, yet simple technique
provides a pulse-by-pulse visual indication of waveform signal
quality, without requiring the user to perform complex signal analysis
during critical patient care situations.
Two AAA battery cells power the 950 and operate it for
approximately 1,600 spot checks
between battery replacement. When the batteries are low, the digital
displays will blink once per second. (Refer to page 9 for battery
specifications and page 10 for battery replacement instructions.)
a
or 18 hours of continuous operation
) in
English
a
Calculated at 40 seconds per spot check using two AAA alkaline battery
cells.
3
N
The 950 at a Glance
%SpO2 Display
Heart Rate Display
Perfusion Display
Finger Grip
Figure 1. Top digital display illustration and bottom label.
Serial
umber
Battery
Polarity
Markings
4
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