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From 5 to 10 days
Last updated: 18 October 2026
Luniv™ is a wellness device using gentle electrical stimulation. It is not a medical device and is not intended to diagnose, treat or prevent sleep apnoea or any other disease.
| Item | Details |
|---|---|
| Name | Luniv™ Anti-Snoring Device |
| Reference | ZHQ-017 |
| Manufacturer | Wenzhou Daisheng Electronic Technology Co., Ltd., No. 35 Bada Road, Linyang, Nanbin Street, Ruian City, Wenzhou, Zhejiang, China – samantha_iparts@163.com |
| Responsible person in the EU | E-CrossStu GmbH (EU authorised representative), Mainzer Landstr. 69, 60329 Frankfurt am Main, Germany – E-CrossStu@web.de |
| Markings | Manufacturer’s EU Declaration of Conformity dated 5 August 2026 (Directives 2014/30/EU and 2011/65/EU). Tests performed: electromagnetic compatibility (Directive 2014/30/EU) and RoHS (Directive 2011/65/EU), Ningbo KPL reports no. KPL2312018980593Y-1EC and -1RC dated 17 March 2023 |
The declaration of conformity is available on request from support@lunivhealth.com.
If in doubt, or if you have a health condition, ask your doctor before use.
Loud, regular snoring, pauses in breathing during sleep or severe daytime tiredness can be signs of sleep apnoea. If this applies to you, see a healthcare professional. Luniv™ does not replace medical treatment.
Do not dispose of the device with household waste. Take it to a collection point for electrical and electronic equipment.
support@lunivhealth.com – include your order number and describe the incident.