| Primary Device ID | 07613327459296 |
| NIH Device Record Key | 97e1a97c-c859-4461-b31b-f2b19216e287 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VC-701 |
| Version Model Number | INC-11648 |
| Catalog Number | INC-11648 |
| Company DUNS | 042405446 |
| Company Name | Stryker Corporation |
| 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 |
| Phone | +1(855)916-3876 |
| NVCustomerService@stryker.com |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327459296 [Primary] |
| NRY | CATHETER, THROMBUS RETRIEVER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-11-26 |
| Device Publish Date | 2018-10-26 |
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| 07613327648546 - Surpass Elite | 2025-03-17 Flow Diverter System |
| 07613327648553 - Surpass Elite | 2025-03-17 Flow Diverter System |