Dynarex Resp-O2 Oxygen E-Cylinder with Post Valve

GUDID 00840117326125

DYNAREX CORPORATION

Oxygen refillable cylinder

• Primary Device ID: 00840117326125
• NIH Device Record Key: 4310722b-822e-4a35-aae6-d4a32466edc8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dynarex Resp-O2 Oxygen E-Cylinder with Post Valve
• Version Model Number: 36390
• 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: false
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117326125 [Primary]

FDA Product Code

• ECX: Cylinder, Compressed Gas, And Valve

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: 2023-04-03
• Device Publish Date: 2023-03-24

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• 00616784191119 - DynaFit Graduated Compression Anti-Embolism Stocking, Medium Knee: 2025-10-06
• 00616784191218 - DynaFit Graduated Compression Anti-Embolism Stocking, Large Knee: 2025-10-06
• 00616784191317 - DynaFit Graduated Compression Anti-Embolism Stocking, X-Large Knee: 2025-10-06