Identity
- Trade Name
- Bio-Console® FDA UDI
- Generic Name
- Cardiopulmonary bypass system centrifugal pump drive unit FDA UDI
- Device Name
- CONSOLE 560BCS1 CONTROL W/SAFETY MEE NR FDA UDI
- Model / Reference
- 560BCS1 FDA UDI
- Description
- CONSOLE 560BCS1 CONTROL W/SAFETY MEE NR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000135447 FDA UDI
- 510(k) Number
- K080824 FDA UDI
- FDA Product Code
- DWA FDA UDI
- GMDN Term
- Cardiopulmonary bypass system centrifugal pump drive unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4380 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cardiopulmonary bypass system centrifugal pump drive unit
Bio-Console® by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiopulmonary bypass system centrifugal pump drive unit.
- Anivia SG1000 Pump Console — Asia Pacific Medical Technology Development Company Limited · Class II
- Anivia SG1000 Pump Console — Apmtd, Inc. · Class II
- Sarns™ Centrifugal System — Terumo Cardiovascular Systems Corporation · Class II
- Anivia SG1000 Pump Console — Apmtd, Inc. · Class II
- INSPIRA ART100 — Inspira Technologies Oxy B.H.N. , Ltd. · Class II
- Terumo® Advanced Perfusion System 1 — Terumo Cardiovascular Systems Corporation · Class II
- Sarns™ Centrifugal System — Terumo Cardiovascular Systems Corporation · Class II
- METAL LOCKING FEATURE FOR CENTRIMAG MOTOR — Thoratec Switzerland GmbH · Class II
Cleared under the same submission
K080824 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI d7b2f118-2d9c-4537-befb-c348fe09ebdd 36 fields · synced May 31, 2026