Neumona
by Neurostimulation Medtech Private Limited 3 variants
Neumona is a Class II device made by Neurostimulation Medtech Private Limited, listed in FDA GUDID since 18 Aug 2025 (UDI-DI 08908006064250), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08908006064250 | Date18 Aug 2025 | StatusListed |
Official records
- AccessGUDID record 08908006064250
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Acupuncture electrical stimulation system
- Model / reference
- NEUMONA
- Primary DI / UDI-DI
- 08908006064250
- FDA product code
- NHI
- GMDN term
- Acupuncture electrical stimulation system
- Device class
- Class II
- Regulation number
- 882.5890
- GUDID distribution status
- In Commercial Distribution
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