Resp-O2 Corrugated Tubing 6' (1.8m),Segmented,Blue

GUDID 00840117326071

Dynarex Corporation

Inhalation-therapy adaptor, single-use

• Primary Device ID: 00840117326071
• NIH Device Record Key: 12a56851-bb93-48cb-9540-ee78a4d66520
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Resp-O2 Corrugated Tubing 6' (1.8m),Segmented,Blue
• Version Model Number: 34123
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117326064 [Primary]
GS1	00840117326071 [Package]; Contains: 00840117326064; Package: Case [50 Units]; In Commercial Distribution

FDA Product Code

• BYX: Tubing, Pressure And Accessories

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: 2024-10-22
• Device Publish Date: 2024-10-14