Codan

GUDID 00813153021477

Extension Set with 3 Gang Valve Manifold

CODAN US CORPORATION

Intravenous administration tubing extension set

• Primary Device ID: 00813153021477
• NIH Device Record Key: 1a3d6f76-319c-464d-bc5c-47dc651706d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Codan
• Version Model Number: W21128
• 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: false
• 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	00813153021477 [Package]; Contains: 10813153021474; Package: [1 Units]; In Commercial Distribution
GS1	10813153021474 [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: 2020-11-09
• Device Publish Date: 2020-10-31

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