QDC-PRO Kit 514011

GUDID 15694311110736

Nox Medical ehf.

Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph
Primary Device ID15694311110736
NIH Device Record Keybf1878c6-201f-40e0-9725-a443f926da58
Commercial Distribution StatusIn Commercial Distribution
Brand NameQDC-PRO Kit
Version Model NumberNOX-QDCPETL_KIT1
Catalog Number514011
Company DUNS365741462
Company NameNox Medical ehf.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kittrue
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

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
GS115694311110736 [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 Number2
Public Version Date2018-03-29
Device Publish Date2016-09-16

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