Argyle
- Primary DI
- 00884521063207
- Brand
- Argyle
- Company
- Cardinal Health, Inc.
- Model
- 8888590224
- Catalog number
- 8888590224
- Device description
- Left Ventricular Sump Vent Catheter
- Published
- 2016-09-24
- 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
Product Codes
| Code | Name |
|---|
| DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| DWF | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00884521063207 | Package | GS1 | 10 | In Commercial Distribution |
| 10884521063204 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00884521063207 | 00884521063207 | 884521063207 | 0884521063207 |
| 10884521063204 | 10884521063204 | | |
GMDN Terms
| Term | Definition |
|---|
| Cardiac ventriculography catheter | A flexible tube with specific tip configurations designed to enter the left or right ventricle to perform diagnostic haemodynamic/angiographic procedures with contrast media. The distal tip may have an end hole and/or several side holes. The tube is introduced into a peripheral blood vessel and its distal tip is placed in the left or right ventricle according to the desired ventriculography. Left ventriculography is used to assess impairment of the left ventricle, the presence of ventricular aneurysms or septal defects, or to assess the mitral valve. Right ventriculography is used mostly to asses congenital heart disease. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Catheter Gauge | 20 | French |
| Length | 20 | Inch |
Storage And Handling
| Type | Low | High | Condition |
|---|
| Special Storage Condition, Specify | 0 | 0 | Keep dry;AVOID DIRECT SUNLIGHT |
Regulatory Flags
- DUNS number
- 080935429
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- 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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