Quantum PureFlow Cardioplegia Heat Exchanger High Flow 1/4 W

GUDID 18051160302267

SPECTRUM MEDICAL SRL

Cardiopulmonary bypass system heat exchanger, single-use

• Primary Device ID: 18051160302267
• NIH Device Record Key: cf046805-776f-44a0-a8e8-b39ec920341f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quantum PureFlow Cardioplegia Heat Exchanger High Flow 1/4 W
• Version Model Number: HX32V-C0W
• Company DUNS: 436188505
• Company Name: SPECTRUM MEDICAL SRL
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	18051160302267 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220110

FDA Product Code

• DTR: Heat-Exchanger, Cardiopulmonary Bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-27
• Device Publish Date: 2024-11-19

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