CAPIOX® VENOUS RESERVOIR

GUDID 34987350706691

TERUMO CORPORATION

Cardiotomy reservoir

• Primary Device ID: 34987350706691
• NIH Device Record Key: a1c06c77-3a3d-4a54-985f-fef939f43b4f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPIOX® VENOUS RESERVOIR
• Version Model Number: CX*VRA1001T2
• Company DUNS: 690543319
• Company Name: TERUMO 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

Customer Support Contacts

• Phone: 1-800-521-2818
• Email: cvscustomerservice@terumomedical.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Fragile. This way up. Keep away from sunlight. Keep away from rain.
• Special Storage Condition, Specify: Between 0 and 0 *Fragile. This way up. Keep away from sunlight. Keep away from rain.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987350706690 [Primary]
GS1	34987350706691 [Package]; Contains: 04987350706690; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• DTM: Filter, Blood, Cardiopulmonary Bypass, Arterial Line

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: 2020-01-22
• Device Publish Date: 2015-09-15

On-Brand Devices [CAPIOX® VENOUS RESERVOIR]

• 34987350706691: CX*VRA1001T2
• 34987350706592: CX*VRA0701T2
• 34987350706493: CX*VRA0401T2
• 34987350706394: CX*VRA0101T2