| Primary Device ID | 07613327303605 |
| NIH Device Record Key | af82f398-84e4-4b15-86fe-2836c33239b7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Switchpoint Infinity |
| Version Model Number | 0678001400 |
| Catalog Number | 0678-001-400 |
| Company DUNS | 078807493 |
| Company Name | STRYKER COMMUNICATIONS 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 | false |
| Lot Batch | false |
| Serial Number | true |
| 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)726-3705 |
| SCC-CS2@stryker.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327303605 [Primary] |
| OCS | Endoscopic video imaging system/component, gastroenterology-urology |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-11-07 |
| 07613327661194 - In-Light Camera | 2025-09-04 |
| 07613327054507 - FLEXIS | 2023-06-15 |
| 07613327589344 - OPERON | 2022-03-30 Pad Set 20" Leg, W Cutout, 3" |
| 07613327054286 - NA | 2020-08-06 Suspension, Navigation System, 10' |
| 07613327054293 - NA | 2020-08-06 Suspension, Navigation System |
| 07613327054514 - NA | 2020-08-06 Medium-Duty Dual Yoke |
| 07613327054521 - NA | 2020-08-06 Medium-Duty Suspension |
| 07613327054538 - NA | 2020-08-06 Light-Duty Suspension |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SWITCHPOINT INFINITY 78294029 2946768 Live/Registered |
STRYKER CORPORATION 2003-08-29 |