Lantronix SLPV1611E-02 Guide de l'utilisateur télécharger pdf (Page 4)

Life-Support Policy

As a general policy, Lantronix does not recommend the use of any of its products in

the following situations:

 Life-support applications where failure or malfunction of the Lantronix product

can be reasonably expected to cause failure of the life-support device or to

significantly affect its safety or effectiveness.

 Direct patient care.

Lantronix will not knowingly sell its products for use in such applications unless it

receives in writing assurances satisfactory to Lantronix that:

 The risks of injury or damage have been minimized,

 The customer assumes all such risks, and

 The liability of Lantronix is adequately protected under the circumstances.

The term life-support device includes but is not limited to neonatal oxygen analyzers,

nerve stimulators (whether used for anesthesia, pain relief or other purposes), auto-

transfusion devices, blood pumps, defibrillators, arrhythmia detectors and alarms,

pacemakers, hemodialysis systems, peritoneal dialysis systems, neonatal ventilator

incubators, ventilators (for adults or infants), anesthesia ventilators, infusion pumps,

and any other devices designated as “critical” by the U.S. FDA.

The information in this guide may change without notice. The manufacturer assumes

no responsibility for any errors that may appear in this guide.

For the latest revision of this product document, please check our online

documentation at

www.lantronix.com/support/documentation.html.

Date Rev. Comments

12/2004 A Initial Document

5/2006 B Part number changes related to RoHS.

1/2009 C Updated entire document, added RoHS changes.

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Lantronix SLPV1611E-02 Guide de l'utilisateur Page 4