DUO - DUO-VENT 2R8404

GUDID 50085412676635

Solution Set with DUO-VENT Spike

BAXTER HEALTHCARE CORPORATION

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• Primary Device ID: 50085412676635
• NIH Device Record Key: 63c6e48d-2286-430c-bdb0-a7751110dbe9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUO - DUO-VENT
• Version Model Number: 2R8404
• Catalog Number: 2R8404
• Company DUNS: 005083209
• Company Name: BAXTER HEALTHCARE 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: medinfo_medproducts@baxter.com

Device Dimensions

• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter
• Total Volume: 5.9 Milliliter
• Length: 1.1 Meter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00085412676630 [Primary]
GS1	50085412676635 [Package]; Contains: 00085412676630; Package: CA [48 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180739

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: 2023-07-19
• Device Publish Date: 2023-07-11

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