Natus 222-435000
by Natus Neurology Incorporated
Natus 222-435000 is a Class II device made by Natus Neurology Incorporated, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00382830038461), 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 | Number00382830038461 | Date16 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00382830038461
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Natus
- Generic name
- Electroencephalograph
- Model / reference
- 222-435000
- Primary DI / UDI-DI
- 00382830038461
- FDA product code
- GWQ
- GMDN term
- Electroencephalograph
- Device class
- Class II
- Regulation number
- 882.1400
- GUDID distribution status
- In Commercial Distribution
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