Medtronic Surestream User manual

1

PN 011045F

Products for Non-Intubated Patients

Directions for Use

ETCO

2

SAMPLING

CO

2

Oral/Nasal

Sampling with O

2

CO

2

Oral/

Nasal

Sampling

with O

2

CO

2

Oral/

Nasal

Sampling

CO

2

Nasal

Sampling

CO

2

Nasal

Sampling

with O

2

O

2

O

2

≤ 5 L/min

2

en

Surestream

TM

EtCO

2

Sampling

for Non-Intubated Patients

Single patient use, not to be re-processed.

Non-sterile / non-pyrogenic.

Does not contain natural rubber latex

Warning: Loose or damaged connections may compro-

mise ventilation or cause an inaccurate mea-

surement of respiratory gases. Securely connect

all components and check connections for leaks

according to standard clinical procedures.

Warning: Do not cut or remove any part of the sample

line. Cutting the sample line could lead to er-

roneous readings.

Warning: Check CO

2

and O

2

tubing regularly during use to

ensure that no kinks are present. Kinked tubing

may cause inaccurate CO

2

sampling or affect O

2

delivery to patient.

Caution: Ensure that tubing is not stretched during use.

Caution: Do not attempt to clean, disinfect, sterilize or

ush any part of the sampling line as this can

cause damage to the monitor.

Caution: Dispose of sampling lines according to standard

operating procedures or local regulations for the

disposal of contaminated medical waste.

Caution: Use of a CO

2

sampling line with H in its name

(indicating that it is for use in humidied envi-

ronments) during MRI scanning may cause in-

terference. These sampling lines include Smart

SureLine Plus H O

2

and SureLine H O

2

. The use

of non H sampling lines is advised.

Note: Replace the sampling line according to hospital

protocol or when a blockage is indicated by the

device. Excessive patient secretions or a build-

up of liquids in the airway tubing may occlude

the sampling line, requiring more frequent re-

placement.

Federal law (U.S.) restricts this device to sale by or on the

order of a physician.

Do not reuse

Does not contain natural rubber latex

Fire Hazard

Storage temperature

Rx Only

Caution, consult accompanying documents

CE Mark

ONLY

Does not

contain natural

rubber latex

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28

Oridion Medical 1987 Ltd.

Har Hotzvim Science-

Based Industrial Park

P.O. Box 45025

Jerusalem 91450, Israel

Tel: 972-2-589-9111

Fax: 972-2-582-5873

Oridion Capnography Inc.

Needham MA 02494

USA

Tel: (781) 453-0500

Toll Free: 1-800-ORIDION

Obelis S.A.

Av. De Tervuren, 34 Bte. 44

B-1040 Brussels

Belgium

Tel: +32.2.34.33.87

This product is covered by one or more

of the following US patents: 6,422,240;

5,857,461; 6,437,316 6,926,005;

5,657,750; 7,383,839; 7,500,483;

6,783,573; and their foreign equivalents.

Additional patent applications pending.

www.oridion.com

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