Niagara catheter
- Primary DI
- 20801741045589
- Brand
- Niagara catheter
- Company
- Bard Access Systems, Inc.
- Model
- 5593240
- Catalog number
- 5593240
- Device description
- 13.5Fr Niagara ST 24cm Kit
- Published
- 2015-11-06
- 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 |
|---|
| MPB | CATHETER, HEMODIALYSIS, NON-IMPLANTED |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| MPB | Catheter, Hemodialysis, Non-Implanted | Gastroenterology, Urology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 10801741045582 | Package | GS1 | 5 | In Commercial Distribution |
| 20801741045589 | Package | GS1 | 10 | In Commercial Distribution |
| 00801741045585 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 10801741045582 | 10801741045582 | | |
| 20801741045589 | 20801741045589 | | |
| 00801741045585 | 00801741045585 | 801741045585 | 0801741045585 |
GMDN Terms
| Term | Definition |
|---|
| Double-lumen haemodialysis catheter, implantable | A sterile, implantable, flexible, double-lumen tube intended to be used for chronic or long-term (> 30 days) vascular access, primarily during haemodialysis, to conduct blood from a patient and returning it after extracorporeal circulation; it may also be used during haemoperfusion and/or apheresis. It is intended for coaxial flow of blood, may be radiopaque, coated with heparin to prevent thrombus formation, and/or include a silver-coated sleeve to retard bacterial growth; devices dedicated to catheter introduction/function (e.g., introducer needle) may be included. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Catheter Gauge | 13.5 | French |
| Length | 24 | Centimeter |
Regulatory Flags
- DUNS number
- 044611812
- 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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