Surge Cardiovascular ANT-1014
Surge Cardiovascular ANT-1014 is a cardioplegia cannula (FDA Class II; FDA product code DWF, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass) made by Med Michigan Holdings LLC, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00817278011023), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00817278011023 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00817278011023
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Surge Cardiovascular
- Generic name
- Cardioplegia cannula
- Model / Ref / Catalog
- ANT-1014
- Primary DI / UDI-DI
- 00817278011023
- FDA product code
- DWF
- GMDN term
- Cardioplegia cannula
- Device class
- Class II
- Regulation number
- 870.4210
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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