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Sleep Profiler

FDA UDI

Class II (US FDA UDI)

by Advanced Brain Monitoring, Inc.

Identity

Trade Name
Sleep Profiler FDA UDI
Generic Name
Electroencephalograph FDA UDI
Device Name
Sleep Profiler System Kit - TRL FDA UDI
Model / Reference
SP40-1003 FDA UDI
Description
Sleep Profiler System Kit - TRL FDA UDI

Identifiers

Primary DI / UDI-DI
00851113007741 FDA UDI
510(k) Number
K152040 FDA UDI
FDA Product Code
OLV FDA UDI
OMC FDA UDI
GMDN Term
Electroencephalograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electroencephalograph

Sleep Profiler by Advanced Brain Monitoring, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroencephalograph.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 925d72eb-a14c-4f6f-ab7c-c8919dc67cf2 35 fields · synced Jun 8, 2026