Resp-O2 Suction Catheter Kit, 10 FR

GUDID 00840711309111

Resp-O2 Suction Catheter Kit, 10 FR, Sterile, 1 Adult Graduated Catheter with Control Valve, 1 Pair of Powder-Free Vinyl Exam Gloves, 1 Pop-Up Basin

DYNAREX CORPORATION

Secretion suction kit Secretion suction kit Secretion suction kit Secretion suction kit Secretion suction kit Secretion suction kit

• Primary Device ID: 00840711309111
• NIH Device Record Key: ec18fbe8-ce52-47b5-9e39-1b3be4b07bf0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Resp-O2 Suction Catheter Kit, 10 FR
• Version Model Number: 32052
• 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: 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	00840117309128 [Package]; Package: Case [50 Units]; In Commercial Distribution
GS1	00840711309111 [Primary]

FDA Product Code

• BSY: Catheters, Suction, Tracheobronchial

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-18
• Device Publish Date: 2022-05-10

On-Brand Devices [Resp-O2 Suction Catheter Kit, 10 FR]

• 00840711309111: Resp-O2 Suction Catheter Kit, 10 FR, Sterile, 1 Adult Graduated Catheter with Control Valve, 1 P
• 00840117309111: Resp-O2 Suction Catheter Kit, 10 FR, Sterile, 1 Adult Graduated Catheter with Control Valve, 1 P