Kabi Access Infusion Sets

GUDID 00813153028001

Manifold 2 Port 4-way stopcocks and rotating male Luer-lock

Codan US Corporation

Intravenous line stopcock

• Primary Device ID: 00813153028001
• NIH Device Record Key: 31577e8e-514a-426a-91ca-7d0f4dfe7692
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kabi Access Infusion Sets
• Version Model Number: FK70110K
• Company DUNS: 058027475
• Company Name: Codan US Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813153028001 [Package]; Contains: 10813153028008; Package: Multivac packaging [1 Units]; In Commercial Distribution
GS1	10813153028008 [Primary]

FDA Product Code

• FPA: Set, Administration, Intravascular

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: 2025-09-04
• Device Publish Date: 2025-08-27

On-Brand Devices [Kabi Access Infusion Sets]

• 00813153028018: Manifold 4 Port 4-way Stopcocks on a manifold plate
• 00813153028001: Manifold 2 Port 4-way stopcocks and rotating male Luer-lock
• 00813153027981: Short Extension Set T-Connector
• 00813153027967: Stopcock 4-way stopcock with rotating Luer-lock