Natus 046782-W
by Xltek
Natus 046782-W is a Class II device made by Xltek, listed in FDA GUDID since 15 Oct 2026 (UDI-DI 00382830063920), registry data as of 2 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00382830063920 | Date15 Oct 2026 | StatusListed |
Official records
- AccessGUDID record 00382830063920
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Natus
- Generic name
- Analytical scalp electrode, single-use
- Model / reference
- 046782-W
- Primary DI / UDI-DI
- 00382830063920
- FDA product code
- GXY
- GMDN term
- Analytical scalp electrode, single-use
- Device class
- Class II
- Regulation number
- 882.1320
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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