LABEL PRODUCT -CODAN

GUDID 00813153022955

Bifurcated Blood Set with Spin-lock

Codan US Corporation

Blood transfusion set, non-exchange

• Primary Device ID: 00813153022955
• NIH Device Record Key: 0a67fc60-7fec-4689-be87-2e3aac6bdf66
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LABEL PRODUCT -CODAN
• Version Model Number: B 870
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813153022955 [Package]; Contains: 10813153022952; Package: Chevron Pouch [1 Units]; In Commercial Distribution
GS1	10813153022952 [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: 2025-06-09
• Device Publish Date: 2025-05-30

On-Brand Devices [LABEL PRODUCT -CODAN]

• 00813153022672: Extension Set with Needle Valve & Needlefree T-connector
• 00813153022344: Extension Set with Spin-Lock
• 10813153028039: One Way Stopcock with Rotating Male Luer lock
• 00813153022955: Bifurcated Blood Set with Spin-lock
• 00813153021613: IV Extension Set with Stopcock, Injection Sites, & T-connector