Resp-O2 Oxygen CO2 Elongated Mask and CO2 Sampling Line

GUDID 00840117316034

Resp-O2 Oxygen CO2 Elongated Pediatric Mask, CO2 Sampling Line 2 with a filter, 7' (2.1m) Oxygen Tube; male/male connector

DYNAREX CORPORATION

Capnography sampling adaptor

• Primary Device ID: 00840117316034
• NIH Device Record Key: bee1af48-c209-4a6d-8c2e-0231b7fe6284
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Resp-O2 Oxygen CO2 Elongated Mask and CO2 Sampling Line
• Version Model Number: 33081
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• 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	00840117316034 [Package]; Contains: 00840117316119; Package: Case [25 Units]; In Commercial Distribution
GS1	00840117316119 [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: 2021-04-30
• Device Publish Date: 2021-04-22

On-Brand Devices [Resp-O2 Oxygen CO2 Elongated Mask and CO2 Sampling Line]

• 00840117316126: Resp-O2 Oxygen CO2 7' (2.1m) Sampling Line; female/female connector
• 00840117316034: Resp-O2 Oxygen CO2 Elongated Pediatric Mask, CO2 Sampling Line 2 with a filter, 7' (2.1m) Oxygen
• 00840117316027: Resp-O2 Oxygen CO2 Elongated Adult Mask, CO2 Sampling Line w/ Filter, 7' (2.1m) Oxygen Tube; Mal