NanoCross™ Elite
- Primary DI
- 00821684066201
- Brand
- NanoCross™ Elite
- Company
- Covidien LP
- Model
- AB14W020210150
- Device description
- PTA AB14W020210150 NANOCROSS 014 V04
- Published
- 2016-04-15
- 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
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| LIT | Catheter, angioplasty, peripheral, transluminal |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| LIT | Catheter, Angioplasty, Peripheral, Transluminal | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00821684066201 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00821684066201 | 00821684066201 | 821684066201 | 0821684066201 |
GMDN Terms
| Term | Definition |
|---|---|
| Peripheral angioplasty balloon catheter, basic | A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 210 | Millimeter |
| Outer Diameter | 2 | Millimeter |
Storage And Handling
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Keep away from sunlight |
| Special Storage Condition, Specify | 0 | 0 | Keep dry |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags
- DUNS number
- 968903703
- 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
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 20884521841700 | Shiley | 70FXLTCD | 2026-03-16 | |
| 20884521841717 | Shiley | 80FXLTCD | 2026-03-16 | |
| 20884521841731 | Shiley | 60FXLTCP | 2026-03-16 | |
| 20884521841748 | Shiley | 70FXLTCP | 2026-03-16 | |
| 20884521841755 | Shiley | 80FXLTCP | 2026-03-16 | |
| 20884521841762 | Shiley | 50FXLTUD | 2026-03-16 | |
| 20884521841779 | Shiley | 60FXLTUD | 2026-03-16 | |
| 20884521841786 | Shiley | 70FXLTUD | 2026-03-16 | |
| 20884521841793 | Shiley | 80FXLTUD | 2026-03-16 | |
| 20884521841809 | Shiley | 50FXLTUP | 2026-03-16 | |
| 20884521841816 | Shiley | 60FXLTUP | 2026-03-16 | |
| 20884521841823 | Shiley | 70FXLTUP | 2026-03-16 | |
| 20884521841830 | Shiley | 80FXLTUP | 2026-03-16 | |
| 30884521841844 | Shiley | 50FXLTIN | 2026-03-16 | |
| 20884521841854 | Shiley | 60FXLTIN | 2026-03-16 | |
| 20884521841861 | Shiley | 70FXLTIN | 2026-03-16 |
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