ViperWire VPR-GW-200
GUDID 30852528005224
VIPERWIRE, ADVANCED, .012" DIA .012" SPRING TIP, 200CM, 5 PACK
Cardiovascular Systems, Inc.
Peripheral vascular guidewire, manual| Primary Device ID | 30852528005224 |
| NIH Device Record Key | 782c56b9-bb26-4a5f-a48c-4fc828810b0c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ViperWire |
| Version Model Number | VPR-GW-200 |
| Catalog Number | VPR-GW-200 |
| Company DUNS | 024954518 |
| Company Name | Cardiovascular Systems, Inc. |
| 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 | true |
| 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
Device Dimensions
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 200 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10852528005220 [Primary] |
| GS1 | 30852528005224 [Package] Contains: 10852528005220 Package: Box [5 Units] In Commercial Distribution |
FDA Product Code
| MCW | Catheter, Peripheral, Atherectomy |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
[30852528005224]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2021-12-22 |
| Device Publish Date | 2015-12-04 |
Devices Manufactured by Cardiovascular Systems, Inc.
| 10852528005206 - Diamondback Peripheral | 2025-06-19 DIAMONDBACK PERIPHERAL, MICRO CROWN, 1.25MM, 60CM SHAFT |
| 10852528005213 - Diamondback Peripheral | 2025-06-19 DIAMONDBACK PERIPHERAL, SOLID CROWN, 1.25MM, 60CM SHAFT |
| 10852528005237 - Diamondback Peripheral | 2025-06-19 DIAMONDBACK PERIPHERAL, SOLID CROWN, 1.50MM, 145CM SHAFT |
| 10852528005244 - Diamondback Peripheral | 2025-06-19 DIAMONDBACK PERIPHERAL, SOLID CROWN, 1.25MM, 145CM SHAFT |
| 10852528005251 - Diamondback Peripheral | 2025-06-19 DIAMONDBACK PERIPHERAL, CLASSIC CROWN, 1.50MM, 145CM SHAFT |
| 10852528005268 - Diamondback Peripheral | 2025-06-19 DIAMONDBACK PERIPHERAL, CLASSIC CROWN, 2.00MM, 145CM SHAFT |
| 10852528005282 - Diamondback Peripheral | 2025-06-19 DIAMONDBACK PERIPHERAL, MICRO CROWN, 1.25MM, 145CM SHAFT |
| 10852528005350 - Diamondback Peripheral | 2025-06-17 Diamondback Peripheral, Radial Access OAD, 1.25mm, 10mm, 200cm shaft |
Trademark Results [ViperWire]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VIPERWIRE 77210006 3644144 Live/Registered |
Cardiovascular Systems, Inc. 2007-06-19 |
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