GUEDEL AIRWAY, SIZE 2, ISO 8

GUDID 05030267040698

GUEDEL AIRWAY, SIZE 2, ISO 8

Intersurgical Incorporated

Oropharyngeal airway, single-use
Primary Device ID05030267040698
NIH Device Record Key9edb18fc-4545-4a87-bf08-589cf38de0b5
Commercial Distribution StatusIn Commercial Distribution
Brand NameGUEDEL AIRWAY, SIZE 2, ISO 8
Version Model Number1112080
Company DUNS785952607
Company NameIntersurgical Incorporated
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com
Phone3154512900
Emailsupport@intersurgicalinc.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105030267040698 [Package]
Contains: 05030267050659
Package: [100 Units]
In Commercial Distribution
GS105030267050659 [Primary]

FDA Product Code

CAEAirway, Oropharyngeal, Anesthesiology

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-02
Device Publish Date2023-05-25

Devices Manufactured by Intersurgical Incorporated

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00816472020558 - Breathing Circuit2025-02-11 Breathing Circuit, 22mm, nonconductive, single use, MRI Safe
00816472020695 - Convenience Pack with 12" Flex Tube2025-02-11 Convenience Pack with 12" Flex Tube
00816472021852 - Sentri Intersurgical EcoLite, adult, mask with CO2 monitoring line2025-02-11 Sentri Intersurgical EcoLite, adult, mask with CO2 monitoring line with universal connector tube, 1.8m
00816472022217 - Smoothbore breathing system without exhalation port, 22mm, 1.6m2025-02-11 Smoothbore breathing system without exhalation port, 22mm, 1.6m
00816472022538 - Multipac® Anesthesia Breathing System2025-02-11 Multipac® Anesthesia Breathing System
00816472023610 - Smoothbore circuit, 22mm2025-02-11 Smoothbore circuit, 22mm
00816472023696 - Multipac Anesthesia Breathing Circuit2025-02-11 Multipac Anesthesia Breathing Circuit

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