BE Micro Recorder B9700073000
by Eb Neuro SpA
BE Micro Recorder B9700073000 is a Class II device made by Eb Neuro SpA, listed in FDA GUDID since 2 Apr 2019 (UDI-DI 08056446900017), 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 | Number08056446900017 | Date2 Apr 2019 | StatusListed |
Official records
- AccessGUDID record 08056446900017
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- BE Micro Recorder
- Generic name
- Electroencephalographic ambulatory recorder
- Model / reference
- B9700073000
- Primary DI / UDI-DI
- 08056446900017
- FDA product code
- GWQ, GWL, OLV, MNR
- GMDN term
- Electroencephalographic ambulatory recorder
- Device class
- Class II
- Regulation number
- 882.1400, 882.1835, 868.2375
- GUDID distribution status
- In Commercial Distribution
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