Resp-O2 EtCO2 Nasal Sampling Cannula, 14' (4.2 m) O2 and CO2

GUDID 00840117342408

Female Luer Connector, Adult, Universal O2 Tubing Connector

Dynarex Corporation

Nasal oxygen cannula, carbon-dioxide-sampling

• Primary Device ID: 00840117342408
• NIH Device Record Key: a05c9398-3b4d-44e6-9c68-7887f72524c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Resp-O2 EtCO2 Nasal Sampling Cannula, 14' (4.2 m) O2 and CO2
• Version Model Number: 33199-F
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117342392 [Package]; Package: Case [25 Units]; In Commercial Distribution
GS1	00840117342408 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143150

FDA Product Code

• CCK: Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-17
• Device Publish Date: 2025-06-09