MAHURKAR
- Primary DI
- 20884521006512
- Brand
- MAHURKAR
- Company
- Covidien LP
- Model
- 8888135195
- Catalog number
- 8888135195
- Device description
- Acute Dual Lumen Catheter Tray,High Flow Curved Extensions with IC* Components,13.5 Fr/Ch (4.5 mm) x 19.5 cm
- Published
- 2015-08-31
- 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
Contact Domains#
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 |
|---|---|---|---|---|
| 20884521006512 | Package | GS1 | 5 | In Commercial Distribution |
| 10884521006515 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 20884521006512 | 20884521006512 |
| 10884521006515 | 10884521006515 |
GMDN Terms#
| Term | Definition |
|---|---|
| Double-lumen haemodialysis catheter, nonimplantable | A flexible, double-lumen tube intended to be used for short-term (< 30 days) central venous (jugular, subclavian vein) and/or femoral vein 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 and may be radiopaque; 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 | 19.5 | Centimeter |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(508)261-8000 | covidien.udi@covidien.com |
Regulatory Flags#
- DUNS number
- 058614483
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- true
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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