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Natus 046800-W

by Xltek

Natus 046800-W is a Class II device made by Xltek, listed in FDA GUDID since 15 Oct 2026 (UDI-DI 00382830063876), registry data as of 2 Nov 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00382830063876 UDI-DI Date15 Oct 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Natus
Generic name
Analytical scalp electrode, single-use
Model / reference
046800-W
Primary DI / UDI-DI
00382830063876
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

Similar devices

Other devices filed under FDA product code GXY (Electrode, Cutaneous).

Other devices from Xltek

See all devices from Xltek →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)