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Sleep Profiler PSG2

FDA UDI

Class II (US FDA UDI)

by Advanced Brain Monitoring, Inc.

Identity

Trade Name
Sleep Profiler PSG2 FDA UDI
Generic Name
Home-use sleep apnoea recording system FDA UDI
Device Name
Sleep Profiler PSG2 LE Device Kit No Belts (PM3) Swiss FDA UDI
Model / Reference
SP29-1002.LE(SWISS) FDA UDI
Description
Sleep Profiler PSG2 LE Device Kit No Belts (PM3) Swiss FDA UDI

Identifiers

Primary DI / UDI-DI
00850015266997 FDA UDI
510(k) Number
K152040 FDA UDI
FDA Product Code
OMC FDA UDI
OLV FDA UDI
GMDN Term
Home-use sleep apnoea recording system 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: ElectroencephalographHome-use sleep apnoea recording system

Sleep Profiler PSG2 by Advanced Brain Monitoring, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use sleep apnoea recording system.

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 3fd762b0-822e-44c9-a50b-b652b3e43cf5 35 fields · synced Jun 8, 2026