NanoCross™
GUDID 00821684059418
PTA AB14W025120090 NANOCROSS 014 V03
Covidien LP
Peripheral angioplasty balloon catheter, basic| Primary Device ID | 00821684059418 |
| NIH Device Record Key | 5dfd3685-1ed0-4600-b385-87efa8d2f25a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NanoCross™ |
| Version Model Number | AB14W025120090 |
| Company DUNS | 968903703 |
| Company Name | Covidien LP |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
Device Dimensions
| Outer Diameter | 2.5 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
| Length | 120 Millimeter |
| Outer Diameter | 2.5 Millimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00821684059418 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K082854
FDA Product Code
| DQY | CATHETER, PERCUTANEOUS |
| LIT | Catheter, angioplasty, peripheral, transluminal |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-08-09 |
| Device Publish Date | 2016-04-21 |
On-Brand Devices [NanoCross™]
| 00821684059821 | PTA AB14W040210150 NANOCROSS 014 V03 |
| 00821684059814 | PTA AB14W040210090 NANOCROSS 014 V03 |
| 00821684059807 | PTA AB14W040150150 NANOCROSS 014 V03 |
| 00821684059791 | PTA AB14W040150090 NANOCROSS 014 V03 |
| 00821684059784 | PTA AB14W040120150 NANOCROSS 014 V03 |
| 00821684059777 | PTA AB14W040120090 NANOCROSS 014 V03 |
| 00821684059760 | PTA AB14W040080150 NANOCROSS 014 V03 |
| 00821684059753 | PTA AB14W040080090 NANOCROSS 014 V03 |
| 00821684059746 | PTA AB14W040040150 NANOCROSS 014 V03 |
| 00821684059739 | PTA AB14W040040090 NANOCROSS 014 V03 |
| 00821684059722 | PTA AB14W040020150 NANOCROSS 014 V03 |
| 00821684059715 | PTA AB14W040020090 NANOCROSS 014 V03 |
| 00821684059708 | PTA AB14W035210150 NANOCROSS 014 V03 |
| 00821684059692 | PTA AB14W035210090 NANOCROSS 014 V03 |
| 00821684059685 | PTA AB14W035150150 NANOCROSS 014 V03 |
| 00821684059678 | PTA AB14W035150090 NANOCROSS 014 V03 |
| 00821684059661 | PTA AB14W035120150 NANOCROSS 014 V03 |
| 00821684059654 | PTA AB14W035120090 NANOCROSS 014 V03 |
| 00821684059647 | PTA AB14W035080150 NANOCROSS 014 V03 |
| 00821684059630 | PTA AB14W035080090 NANOCROSS 014 V03 |
| 00821684059623 | PTA AB14W035040150 NANOCROSS 014 V03 |
| 00821684059616 | PTA AB14W035040090 NANOCROSS 014 V03 |
| 00821684059609 | PTA AB14W035020150 NANOCROSS 014 V03 |
| 00821684059593 | PTA AB14W035020090 NANOCROSS 014 V03 |
| 00821684059586 | PTA AB14W030210150 NANOCROSS 014 V03 |
| 00821684059579 | PTA AB14W030210090 NANOCROSS 014 V03 |
| 00821684059562 | PTA AB14W030150150 NANOCROSS 014 V03 |
| 00821684059555 | PTA AB14W030150090 NANOCROSS 014 V03 |
| 00821684059548 | PTA AB14W030120150 NANOCROSS 014 V03 |
| 00821684059531 | PTA AB14W030120090 NANOCROSS 014 V03 |
| 00821684059524 | PTA AB14W030080150 NANOCROSS 014 V03 |
| 00821684059517 | PTA AB14W030080090 NANOCROSS 014 V03 |
| 00821684059500 | PTA AB14W030040150 NANOCROSS 014 V03 |
| 00821684059494 | PTA AB14W030040090 NANOCROSS 014 V03 |
| 00821684059487 | PTA AB14W030020150 NANOCROSS 014 V03 |
| 00821684059470 | PTA AB14W030020090 NANOCROSS 014 V03 |
| 00821684059463 | PTA AB14W025210150 NANOCROSS 014 V03 |
| 00821684059456 | PTA AB14W025210090 NANOCROSS 014 V03 |
| 00821684059449 | PTA AB14W025150150 NANOCROSS 014 V03 |
| 00821684059432 | PTA AB14W025150090 NANOCROSS 014 V03 |
| 00821684059425 | PTA AB14W025120150 NANOCROSS 014 V03 |
| 00821684059418 | PTA AB14W025120090 NANOCROSS 014 V03 |
| 00821684059401 | PTA AB14W025080150 NANOCROSS 014 V03 |
| 00821684059395 | PTA AB14W025080090 NANOCROSS 014 V03 |
| 00821684059388 | PTA AB14W025040150 NANOCROSS 014 V03 |
| 00821684059371 | PTA AB14W025040090 NANOCROSS 014 V03 |
| 00821684059364 | PTA AB14W025020150 NANOCROSS 014 V03 |
| 00821684059357 | PTA AB14W025020090 NANOCROSS 014 V03 |
| 00821684059340 | PTA AB14W020210150 NANOCROSS 014 V03 |
| 00821684059333 | PTA AB14W020210090 NANOCROSS 014 V03 |
Trademark Results [NanoCross]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NANOCROSS 86434065 4872926 Live/Registered |
Covidien, LP 2014-10-24 |
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