Neurovirtual Maxxi RIP Thorax Interface 7ft
Neurovirtual Maxxi RIP Thorax Interface 7ft (SI2123) is a polysomnograph (FDA Class II; FDA product code MNR, Ventilatory Effort Recorder) made by Neurovirtual USA, Inc., cleared under FDA 510(k) K171304 on 24 Jun 2019 and listed in FDA GUDID since 26 Nov 2019 (UDI-DI 00850008393112), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850008393112 | Date26 Nov 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK171304 | Date24 Jun 2019 | StatusActive |
Official records
- AccessGUDID record 00850008393112
- FDA 510(k) database K171304
Across registries
- FDA 510(k) K171304 decided 24 Jun 2019 Active
- FDA GUDID UDI-DI 00850008393112 listed 26 Nov 2019 Listed
Timeline
- Cleared FDA 510(k) K171304
- Listed FDA GUDID 00850008393112
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Neurovirtual
- Generic name
- Polysomnograph
- Model / Ref / Catalog
- Maxxi RIP Thorax Interface 7ft, SI2123
- Primary DI / UDI-DI
- 00850008393112
- 510(k) Number
- FDA product code
- MNR
- GMDN term
- Polysomnograph
- Device class
- Class II
- Regulation number
- 868.2375
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices in this category
Other devices filed under Polysomnograph.