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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.
SecureLinx SLP Remote Power Manager 3