| Primary Device ID | 07613327051544 |
| NIH Device Record Key | 73e01bd5-00ad-472f-9a6b-5ee6a191f1e8 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 0233050067 |
| Catalog Number | 0233-050-067 |
| Company DUNS | 187502109 |
| 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 | false |
| 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 |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
| Length | 7.5 Feet |
| Lumen/Inner Diameter | 2 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327051544 [Primary] |
| FCW | Light source, fiberoptic, routine |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327051544]
Hydrogen Peroxide;Moist Heat or Steam Sterilization;Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
| 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 |