Identity
- Trade Name
- Nautilus VF Oxygenator Cable FDA UDI
- Generic Name
- Extracorporeal membrane oxygenator FDA UDI
- Device Name
- The VF cable accessory allows for a low power signal to transmit to the sensors and return the calculated parameters in digital format to another MC3 device, the VitalFlow Console, for digital display purposes. FDA UDI
- Model / Reference
- 58130 FDA UDI
- Description
- The VF cable accessory allows for a low power signal to transmit to the sensors and return the calculated parameters in digital format to another MC3 device, the VitalFlow Console, for digital display purposes. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10850007732421 FDA UDI
- FDA Product Code
- BYS FDA UDI
- GMDN Term
- Extracorporeal membrane oxygenator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Extracorporeal membrane oxygenator
Nautilus VF Oxygenator Cable by Michigan Critical Care Consultants, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Michigan Critical Care Consultants, Inc.
Sources (1)
- FDA UDI 1b003075-6908-4791-b683-2845400affbe 33 fields · synced Jun 6, 2026