Instruction Manual
Forehead Sleep Recorder File No. DMR-SM902-4-25 Ver:A0
4 / 23 Copyright© Shenzhen BrainScience Bio-Info Technology Co., LTD
3. Revision record
Product manual version: A0
Product manual issued date: 2019-06-18
Embeded software name: Umind sleep firmware
Embeded software version:V1.0
Embeded software issued date: 2019-06-05
Application software name: Sleep recorder
Application software version: V1.0
Application software issued date: 2019-06-12
4. Customer Service
Company name: Shenzhen BrainScience Bio-Info Technology Co., LTD
Address: Room 1401, Building 7A, Wanke Yuncheng, Dashi 1 Road, Nanshan District, Shenzhen
City, Guangdong Province, China.
Web site: http://www.eegsmart.com/contact.html
Service phone number: +86-0755-86536023
Mail for Post-sale Service: ma@eegsmart.com
5. Direction for safety
5.1. Warning
1) Do not use it in the place with flammable gas, such as anesthetic. There is danger of
explosion.
2) Do not throw the equipment into fire as it may cause an explosion.
3) Do not connect this product to a patient undergoing cardiac defibrillation.
4) Do not use this product in an MRI environment.
5) Clinicians are advised to instruct users on the proper use of this product.
6) Do not sterilize this product or accessories.
7) Pacemakers or other medical electronic equipment could interfere with the EEG signal and
decrease sleep staging accuracy.
8) The function or safety of this product could be impaired if it has been subjected to
unfavorable conditions or mishandling.
9) If, at any time, function or safety is thought to be impaired, damage to this product or
accessories has been observed/suspected; this product should be taken out of operation and
secured against unintended use. Contact after-sale service.
10) This product is designed for indoor use only. After shipping or transportation, allow this
product to reach operation environment temperature before using.
11) Some users may experience skin irritation, hypersensitivity, or an allergic reaction to the
self-stick sensors or adhesive tape. Advise patient that if this occurs, to discontinue use and