Primary Device ID | 00886874110072 |
NIH Device Record Key | 0a6a370c-6910-4e59-a5b4-15a9abd02fc6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | daVinci S |
Version Model Number | 370193 |
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 | 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 |