| 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 |
| 07613327634914 - Neptune | 2024-04-24 SMART DOCKING STATION (120V) |
| 07613327627664 - KNOTILUS+ | 2024-03-15 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK |
| 07613327627701 - KNOTILUS+ | 2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK |
| 07613327623796 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HIP |
| 07613327623833 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP |
| 07613327634686 - Iconix | 2024-03-12 Iconix DC Guide for 1.4mm anchor |
| 07613327634693 - Iconix | 2024-03-12 |
| 07613327616675 - SPY | 2024-03-06 |