Perfusion Pack
- Primary DI
- 10803622124232
- Brand
- Perfusion Pack
- Company
- LIVANOVA USA, INC.
- Model
- Perfusion Pack
- Published
- 2015-03-13
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 10803622124232 | Package | GS1 | 10 | In Commercial Distribution |
| 00803622124235 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 10803622124232 | 10803622124232 | | |
| 00803622124235 | 00803622124235 | 803622124235 | 0803622124235 |
GMDN Terms
| Term | Definition |
|---|
| Cardiopulmonary bypass system tubing set | A collection of sterile devices including tubing and typically clamps, filters, connectors, and stopcocks, used in a circuit for a cardiopulmonary bypass procedure. The tubing is typically polymeric and may be heparin coated. It is typically used in the blood pump head of a cardiopulmonary bypass system. The tubing, when used in a roller type pump, will be cyclically compressed by the blood pump to cause the blood to flow through the heart-lung bypass system. This is a single-use device. |
Regulatory Flags
- DUNS number
- 080914995
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- true
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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