Intubation Guide Kit

GUDID 00860009615533

AIR Q KIT - SZ 3

Nar Medical Depot, LLC

General surgical procedure kit, non-medicated, single-use
Primary Device ID00860009615533
NIH Device Record Keyd18d6529-2f33-4b26-b37b-284b6e2a69da
Commercial Distribution StatusIn Commercial Distribution
Brand NameIntubation Guide Kit
Version Model Number800-00046
Company DUNS117667182
Company NameNar Medical Depot, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100860009615533 [Primary]

FDA Product Code

OGKOrotracheal Intubation Guide Kit

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-07-23
Device Publish Date2025-07-15

On-Brand Devices [Intubation Guide Kit]

00860009615557AIR Q KIT - SZ 4
00860009615540AIR Q KIT - SZ 5
00860009615533AIR Q KIT - SZ 3

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.