Resp-O2 Closed Suction Endotracheal Catheters, Sterile

GUDID 00840117319509

Adult, T-Piece ( Diameter 5.3mm 16FR ), Length (Endotracheal 54.0cm/21.3in). CONTENTS: Catheter, 22mm Flex Tube, Change of Day.

Dynarex Corporation

Closed-suction breathing circuit connector/switch

• Primary Device ID: 00840117319509
• NIH Device Record Key: 0d515364-513d-4364-a02c-d9276597ab05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Resp-O2 Closed Suction Endotracheal Catheters, Sterile
• Version Model Number: 31023
• 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: true
• Expiration Date: true
• 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	00840117319509 [Primary]
GS1	00840117319516 [Package]; Package: Case [2 Units]; In Commercial Distribution
GS1	00840117338937 [Package]; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• BSY: Catheters, Suction, Tracheobronchial

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2026-01-12
• Device Publish Date: 2021-04-22

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