| Primary Device ID | 00886874110881 |
| NIH Device Record Key | 27ccf562-295b-450f-9064-842b3a74cafe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | daVinci Si |
| Version Model Number | 381103 |
| Company DUNS | 938647021 |
| Company Name | INTUITIVE SURGICAL, 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886874110881 [Primary] |
| IZI | System, x-ray, angiographic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-03-02 |
| Device Publish Date | 2016-07-08 |
| 00886874110881 | FLUORESCENCE IMAGING CAMERA HEAD AND CABLE KIT |
| 00886874110874 | VISION SIDE SYSTEM |
| 00886874110799 | VISION SIDE SYSTEM, RECERTIFIED |
| 00886874110782 | SURGEON SIDE CONSOLE, RECERTIFIED |
| 00886874110775 | PATIENT SIDE CART, RECERTIFIED |
| 00886874110751 | PATIENT SIDE CART, RECERTIFIED |
| 00886874110737 | PATIENT SIDE CART, 4-ARM, RECERTIFIED |
| 00886874110713 | PATIENT SIDE CART, 3-ARM |
| 00886874110690 | PATIENT SIDE CART, 4-ARM |
| 00886874110683 | SURGEON SIDE CONSOLE |