Advance Plus Universal IV Administration Set 1720WY

GUDID 10020221117209

IV Administration Set, Luer Slip, 1 injection site, 20" tubing

Exel International

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• Primary Device ID: 10020221117209
• NIH Device Record Key: aa230c9b-261f-4346-ac16-2f8a5dd5ecf5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advance Plus Universal IV Administration Set
• Version Model Number: 1720WY
• Catalog Number: 1720WY
• Company DUNS: 180572216
• Company Name: Exel International
• 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: false
• 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	00020221117202 [Primary]
GS1	10020221117209 [Package]; Contains: 00020221117202; Package: [100 Units]; In Commercial Distribution

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-11-08
• Device Publish Date: 2016-09-26

On-Brand Devices [Advance Plus Universal IV Administration Set]

• 01002022117307: IV Administration Set, Luer Slip, 1 injection site, 30" tubing
• 10020221117209: IV Administration Set, Luer Slip, 1 injection site, 20" tubing
• 10020221017721: IV Administration Set, 72" tubing
• 10020221017301: IV Administration Set, Luer Lock/Slip, 30" tubing
• 00020221017205: IV Administration Set, Luer Lock/Slip, 20" tubing
• 10020221017127: IV Administration Set, Luer Lock/Slip, 12" tubing