Compumedics Somfit 9037-0013-00

GUDID 09342451002860

Somfit System Americas (7 electrodes)

COMPUMEDICS LIMITED

Polysomnograph
Primary Device ID09342451002860
NIH Device Record Key587fea35-fe71-4e47-9c58-97562bea7be4
Commercial Distribution StatusIn Commercial Distribution
Brand NameCompumedics Somfit
Version Model NumberSomfit
Catalog Number9037-0013-00
Company DUNS753750967
Company NameCOMPUMEDICS LIMITED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au
Phone+61384207386
Emailsupport@compumedics.com.au

Device Identifiers

Device Issuing AgencyDevice ID
GS109342451002860 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MNRVentilatory Effort Recorder

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-20
Device Publish Date2026-03-12

On-Brand Devices [Compumedics Somfit]

09342451002860Somfit System Americas (7 electrodes)
09342451002822Somfit System Americas
09342451002662Somfit Charger
09342451002655Somfit Main Unit

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