← Back to catalogue

Natus

FDA UDI

Class II (US FDA UDI)

by Xltek

Identity

Trade Name
Natus FDA UDI
Generic Name
Analytical scalp electrode, single-use FDA UDI
Device Name
BrainWatch Headband (LG)/10 pack – 55-62 cm FDA UDI
Model / Reference
046796 FDA UDI
Description
BrainWatch Headband (LG)/10 pack – 55-62 cm FDA UDI

Identifiers

Primary DI / UDI-DI
00382830051828 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Analytical scalp electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Analytical scalp electrode, single-use

Natus by Xltek — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical scalp electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Xltek

Sources (1)

  • FDA UDI 9809661c-8e40-4a9a-80b2-fc30a9f4af52 33 fields · synced Jun 1, 2026