CAPIOX XX*XH032

GUDID 54987350734612

Device Holder

TERUMO CORPORATION

Medical device service rail clamp

• Primary Device ID: 54987350734612
• NIH Device Record Key: f4f05fab-53d5-4c8c-b1db-f2c3c5cbdfc2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPIOX
• Version Model Number: XX*XH032
• Catalog Number: XX*XH032
• Company DUNS: 690543319
• Company Name: TERUMO CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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
• Phone: +1(800)521-2818
• Email: cvscustomerservice@terumomedical.com
• Phone: +1(800)521-2818
• Email: cvscustomerservice@terumomedical.com
• Phone: +1(800)521-2818
• Email: cvscustomerservice@terumomedical.com
• Phone: +1(800)521-2818
• Email: cvscustomerservice@terumomedical.com
• Phone: +1(800)521-2818
• Email: cvscustomerservice@terumomedical.com
• Phone: +1(800)521-2818
• Email: cvscustomerservice@terumomedical.com
• Phone: +1(800)521-2818
• Email: cvscustomerservice@terumomedical.com

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987350734617 [Primary]
GS1	54987350734612 [Package]; Contains: 04987350734617; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• KRI: ACCESSORY EQUIPMENT, CARDIOPULMONARY BYPASS

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-07-08
• Device Publish Date: 2022-06-30

On-Brand Devices [CAPIOX]

• 04987350769213: CAPIOX Cardiotomy Reservoir
• 54987350706336: CAPIOX Luer Thermistor
• 54987350705735: CAPIOX Bubble Trap
• 54987350705698: CAPIOX Bubble Trap
• 04987350739100: CAPIOX FX Oxygenator
• 04987350739124: CAPIOX FX Oxygenator
• 04987350739087: CAPIOX FX Oxygenator
• 04987350739063: CAPIOX FX Oxygenator
• 04987350739049: CAPIOX RX Oxygenator
• 04987350739025: CAPIOX RX Oxygenator
• 54987350771839: Device Holder
• 54987350764053: Device Holder
• 54987350764039: Device Holder
• 54987350764015: Device Holder
• 54987350744598: Device Holder
• 04987350742575: Device Holder
• 54987350734650: Device Holder
• 54987350734636: Device Holder
• 54987350734612: Device Holder
• 54987350733677: Device Holder
• 54987350733653: Device Holder
• 54987350703762: Device Holder
• 54987350743256: CAPIOX CARDIOPLEGIA