Noxturnal® 539010

GUDID 15694311110255

Nox Medical ehf.

Sleep disorder interpretive software
Primary Device ID15694311110255
NIH Device Record Keyce8bf2d1-01fe-414e-b5e8-a74f5497adfc
Commercial Distribution StatusIn Commercial Distribution
Brand NameNoxturnal®
Version Model NumberNOX-NOXT_CD
Catalog Number539010
Company DUNS365741462
Company NameNox Medical ehf.
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 Batchtrue
Serial Numberfalse
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

Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS115694311110255 [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 StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-12-11
Device Publish Date2016-09-16

Devices Manufactured by Nox Medical ehf.

15694311111665 - Noxturnal US APP2021-10-26
15694311111610 - Nox A1® EEG 5 Lead Gold Electrode Cable2021-09-15
15694311111627 - Nox A1® EEG Head Cable 2021-09-15
15694311111566 - Nox A1s Recorder2021-07-19
15694311111580 - Nox A1s System2021-07-19
15694311111597 - Nox C1s Kit2021-07-19
15694311111467 - Nox T3s System2021-06-08
15694311110682 - Nox A1 Starter Sensor Kit, Adult2021-02-11

Trademark Results [Noxturnal]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NOXTURNAL
NOXTURNAL
79100410 4219907 Live/Registered
Nox Medical ehf
2011-06-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.