TandemLung LifeSPARC 5830-3631
by Cardiacassist, Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00814112020777 | Date29 May 2020 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- TandemLung LifeSPARC
- Generic Name
- Cardiopulmonary bypass system centrifugal pump
- Model / Reference
- 5830-3631
- Primary DI / UDI-DI
- 00814112020777
- FDA Product Code
- KRI, KFM, DTZ, DRE, DWF, QNR
- GMDN Term
- Cardiopulmonary bypass system centrifugal pump
- Device Class
- Class I
- Regulation Number
- 870.4200, 870.4360, 870.4350, 870.1310, 870.4210, 870.4100
- Commercial Distribution
- Not in Commercial Distribution
- MRI Safety
- MR Unsafe
Other devices from Cardiacassist, Inc.
Properties
Other properties (7)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No