Resp-O2 Nasopharyngeal Airways, 22 FR

GUDID 00840117323315

DYNAREX CORPORATION

Nasopharyngeal airway, single-use
Primary Device ID00840117323315
NIH Device Record Key86c43ba2-0613-4234-bda4-1b489591ce28
Commercial Distribution StatusIn Commercial Distribution
Brand NameResp-O2 Nasopharyngeal Airways, 22 FR
Version Model Number36276
Company DUNS008124539
Company NameDYNAREX CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100840117315297 [Package]
Contains: 00840117315389
Package: Master Shipper [10 Units]
In Commercial Distribution
GS100840117315389 [Package]
Package: Case [10 Units]
In Commercial Distribution
GS100840117323315 [Primary]

FDA Product Code

BTQAirway, Nasopharyngeal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-26
Device Publish Date2022-05-18

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