CAPIOX®RX

GUDID 04987350771056

RX15

TERUMO CORPORATION

Extracorporeal membrane oxygenator

• Primary Device ID: 04987350771056
• NIH Device Record Key: 9bd150a4-af44-4f6d-81d0-a40509df410f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPIOX®RX
• Version Model Number: CX*RX15RW30
• 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

Device Dimensions

• Area/Surface Area: 1.5 Square meter

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	04987350771056 [Primary]

FDA Product Code

• DTZ: Oxygenator, 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: 3
• Public Version Date: 2020-01-22
• Device Publish Date: 2015-09-15

On-Brand Devices [CAPIOX®RX]

• 54987350781852: RX05
• 04987350771216: RX15
• 04987350771193: RX15
• 04987350771094: RX15
• 04987350771070: RX15
• 04987350771056: RX15
• 04987350771032: RX15
• 04987350769572: RX25
• 04987350769558: RX25
• 04987350769534: RX25
• 04987350769510: RX25
• 04987350763495: RX05
• 04987350763471: RX05