| Primary Device ID | 00886874113479 |
| NIH Device Record Key | 9049e661-d8f0-4100-9883-e6969d486fd3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Single-Site; daVinci Si |
| Version Model Number | 428083 |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886874113479 [Primary] |
| NAY | System,surgical,computer controlled instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00886874113479]
Moist Heat or Steam Sterilization
[00886874113479]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 15 |
| Public Version Date | 2020-03-02 |
| Device Publish Date | 2016-09-14 |
| 00886874113479 | DOCK ASSIST TOOL |
| 00886874112113 | WRISTED NEEDLE DRIVER |
| 10886874112103 | FENESTRATED BIPOLAR FORCEPS |
| 00886874112090 | PERMANENT CAUTERY HOOK |
| 00886874112083 | CURVED NEEDLE DRIVER |
| 00886874111963 | CROCODILE GRASPER |
| 00886874111956 | FUNDUS GRASPER |
| 00886874111949 | CURVED SCISSORS |
| 00886874111925 | CADIERE FORCEPS |
| 00886874111918 | SUCTION IRRIGATOR |
| 00886874111901 | CLIP APPLIER, HEM-O-LOK ML |
| 00886874111895 | MONOPOLAR CAUTERY |
| 00886874111888 | MARYLAND DISSECTOR |