Oxitone 1000M
User Manual Rev. 1.
Page 3 of 39
CE Notice
Marking by the CE symbol indicates compliance of this device with the European Medical Device
Directive 93/42/EEC concerning Medical Devices. This non-invasive pulse oximeter is designed
according to the international standard ISO13485:2016, medical devices.
EU authorized representative for Oxitone Medical Ltd.:
MedNet EC-REP GmbH
Borkstraße 10 | 48163 Münster | Germany
www.mednet-eurep.com
UDI: (01) 07290017350004
Rev. Date History Change
1.0 4 April 2020 Initial Document
1.1 16 Aug 2020 Correct and add that under normal conditions, the battery will lose
less than 25% capacity after lasts for approximately 300
charge/discharge cycles instead of 250 charge/discharge cycles.
Correct capacity to Approximately 24 hours after full charge.
Update Logo
1.2 25 Jan 2021 Update EC REP name, Update Logo, Correct UDI, update charger
label and monitor label.
Disclaimer
Information provided by Oxitone Medical Ltd. is believed to be accurate and reliable. However,
Oxitone Medical Ltd. assumes no responsibility for the use of such information, nor for any
infringements of patents or other rights of third parties, that may result from its use.
PLEASE READ THIS USER MANUAL BEFORE OPERATING THE SYSTEM.
To Next Page
Loading...