Be Plus Pro Advanced B9700078004
by Eb Neuro SpA
Be Plus Pro Advanced B9700078004 is a Class II device made by Eb Neuro SpA, cleared under FDA 510(k) K242305 on 4 Sep 2024 and listed in FDA GUDID since 4 Dec 2024 (UDI-DI 08056446900925), 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 | Number08056446900925 | Date4 Dec 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK242305 | Date4 Sep 2024 | StatusActive |
Official records
- AccessGUDID record 08056446900925
- FDA 510(k) database K242305
Across registries
- FDA 510(k) K242305 decided 4 Sep 2024 Active
- FDA GUDID UDI-DI 08056446900925 listed 4 Dec 2024 Listed
Timeline
- Cleared FDA 510(k) K242305
- Listed FDA GUDID 08056446900925
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Be Plus Pro Advanced
- Generic name
- Electroencephalograph
- Model / reference
- B9700078004
- Primary DI / UDI-DI
- 08056446900925
- 510(k) Number
- FDA product code
- GWL, GWQ
- GMDN term
- Electroencephalograph
- Device class
- Class II
- Regulation number
- 882.1835, 882.1400
- GUDID distribution status
- In Commercial Distribution
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