Nautilus VF Oxygenator Cable 48150

GUDID 10850007732322

Power and data cable for the Nautilus VF ECMO Oxygenator

MICHIGAN CRITICAL CARE CONSULTANTS, INC.

Extracorporeal membrane oxygenator

• Primary Device ID: 10850007732322
• NIH Device Record Key: 90e6f32b-c158-4cf2-b6a8-5eb6576e189f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nautilus VF Oxygenator Cable
• Version Model Number: 58130
• Catalog Number: 48150
• Company DUNS: 806687406
• Company Name: MICHIGAN CRITICAL CARE CONSULTANTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10850007732322 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232767

FDA Product Code

• BYS: Oxygenator, Long Term Support Greater Than 6 Hours

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: 2024-09-27
• Device Publish Date: 2024-09-19

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