CAPIOX XX*XH041

GUDID 54987350734636

Device Holder

TERUMO CORPORATION

Medical device service rail clamp Medical device service rail clamp Medical device service rail clamp Medical device service rail clamp Medical device service rail clamp Medical device service rail clamp Medical device service rail clamp Medical device service rail clamp

• Primary Device ID: 54987350734636
• NIH Device Record Key: 7ef18ed6-d2e0-4fe4-b491-9ab7b8b570a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPIOX
• Version Model Number: XX*XH041
• Catalog Number: XX*XH041
• 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	04987350734631 [Primary]
GS1	54987350734636 [Package]; Contains: 04987350734631; Package: [10 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
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• 04987350742575: Device Holder
• 54987350734650: Device Holder
• 54987350734636: Device Holder
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