Capiox® Flexible Venous Reservoir

GUDID 50699753450207

Terumo Cardiovascular Systems Corporation

Cardiotomy reservoir

• Primary Device ID: 50699753450207
• NIH Device Record Key: fadc74fa-1766-41bc-8124-279ec10af7bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Capiox® Flexible Venous Reservoir
• Version Model Number: 3CXFVR1500XC
• Company DUNS: 177655466
• Company Name: Terumo Cardiovascular Systems 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00699753450202 [Primary]
GS1	50699753450207 [Package]; Contains: 00699753450202; Package: 5 Piece Case [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070839

FDA Product Code

• DTN: Reservoir, Blood, Cardiopulmonary Bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-22
• Device Publish Date: 2016-10-06

On-Brand Devices [Capiox® Flexible Venous Reservoir]

• 50699753450207: 3CXFVR1500XC
• 50699753450191: 3CXFVR1500X