← Back to catalogue

Compumedics Somte

FDA UDI

Class II (US FDA UDI)

by Compumedics Limited

Identity

Trade Name
Compumedics Somte FDA UDI
Generic Name
Polysomnograph FDA UDI
Device Name
Somte Recording System Compumedics, no Software FDA UDI
Model / Reference
Somte FDA UDI
Description
Somte Recording System Compumedics, no Software FDA UDI

Identifiers

Catalog Number
9012-0003-01 FDA UDI
Primary DI / UDI-DI
09342451001733 FDA UDI
510(k) Number
K021176 FDA UDI
FDA Product Code
MNR FDA UDI
GMDN Term
Polysomnograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 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: Polysomnograph

Compumedics Somte by Compumedics Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polysomnograph.

Cleared under the same submission

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
Compumedics Limited

Sources (1)

  • FDA UDI e19be9b3-1887-41a6-9e04-d1ad05f214ca 37 fields · synced May 30, 2026