Airtraq

GUDID 08436031030716

Airtraq SP Double Lumen

PRODOL MEDITEC, SA

Channelled video intubation laryngoscope
Primary Device ID08436031030716
NIH Device Record Key4cd015d3-b1af-4dd9-9f2d-5e10f8cd799e
Commercial Distribution StatusIn Commercial Distribution
Brand NameAirtraq
Version Model NumberA-071
Company DUNS541001090
Company NamePRODOL MEDITEC, SA
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108436031030716 [Primary]

FDA Product Code

CCWLaryngoscope, Rigid

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-09
Device Publish Date2023-08-01

On-Brand Devices [Airtraq]

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78436031035017Airtraq Avant Optics
78436031033921Airtraq A-390 WiFi Camera KIT
78436031033907Airtraq A-390 WiFi Camera
08436031030716Airtraq SP Double Lumen
48436031030615Airtraq SP Adult Nasal
48436031030516Airtraq SP Infant Nasal
48436031030417Airtraq SP Infant
48436031030318Airtraq SP Pediatric
48436031030219Airtraq SP Small
48436031030110Airtraq SP Regular

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